Canonical Allele Identifier: CA1777533196
Gene: FGFR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38413763_38413770delinsGGGGGAGT , CM000670.2:g.38413763_38413770delinsGGGGGAGT GRCh38
NC_000008.10:g.38271281_38271288delinsGGGGGAGT , CM000670.1:g.38271281_38271288delinsGGGGGAGT GRCh37
NC_000008.9:g.38390438_38390445delinsGGGGGAGT NCBI36
NG_007729.1:g.60065_60072delinsACTCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000703405.1:c.2327_2334delinsACTCCCCC ENSP00000515291.1:p.Tyr776=
ENST00000341462.9:c.2280+148_2280+155delinsACTCCCCC ENSP00000340636.7:n.2280+148_2280+155delinsACTCCCCC
ENST00000425967.8:c.2280+148_2280+155delinsACTCCCCC ENSP00000393312.4:n.2280+148_2280+155delinsACTCCCCC
ENST00000524528.2:n.3220_3227delinsACTCCCCC
ENST00000682398.1:n.1567_1574delinsACTCCCCC
ENST00000683132.1:n.1130_1137delinsACTCCCCC
ENST00000683765.1:c.2472+148_2472+155delinsACTCCCCC ENSP00000507039.1:n.2472+148_2472+155delinsACTCCCCC
ENST00000683815.1:c.2315_2322delinsACTCCCCC ENSP00000507997.1:p.Tyr772=
ENST00000683948.1:n.3015_3022delinsACTCCCCC
ENST00000684654.1:c.2048_2055delinsACTCCCCC ENSP00000507205.1:p.Tyr683=
ENST00000447712.7:c.2327_2334delinsACTCCCCC MANE Select ENSP00000400162.2:p.Tyr776=
ENST00000649678.1:c.2315_2322delinsACTCCCCC ENSP00000497266.1:p.Tyr772=
ENST00000674189.1:c.*1938+148_*1938+155delinsACTCCCCC ENSP00000501345.1:n.*1938+148_*1938+155delinsACTCCCCC
ENST00000674380.1:c.*2294_*2301delinsACTCCCCC ENSP00000501514.1:n.*2294_*2301delinsACTCCCCC
ENST00000674474.1:n.3821_3828delinsACTCCCCC
ENST00000326324.10:c.2054_2061delinsACTCCCCC ENSP00000327229.6:p.Tyr685=
ENST00000335922.9:c.2297_2304delinsACTCCCCC ENSP00000337247.5:p.Tyr766=
ENST00000341462.8:c.*1377_*1384delinsACTCCCCC ENSP00000340636.6:n.*1377_*1384delinsACTCCCCC
ENST00000356207.9:c.2060_2067delinsACTCCCCC ENSP00000348537.5:p.Tyr687=
ENST00000397091.9:c.2321_2328delinsACTCCCCC ENSP00000380280.5:p.Tyr774=
ENST00000397103.5:c.2060_2067delinsACTCCCCC ENSP00000380292.1:p.Tyr687=
ENST00000397108.8:c.2321_2328delinsACTCCCCC ENSP00000380297.4:p.Tyr774=
ENST00000397113.6:c.2321_2328delinsACTCCCCC ENSP00000380302.2:p.Tyr774=
ENST00000425967.7:c.2420_2427delinsACTCCCCC ENSP00000393312.3:p.Tyr807=
ENST00000447712.6:c.2327_2334delinsACTCCCCC ENSP00000400162.2:p.Tyr776=
ENST00000526570.5:n.4606_4613delinsACTCCCCC
ENST00000526688.1:n.59+148_59+155delinsACTCCCCC
ENST00000531196.5:c.538_545delinsACTCCCCC ENSP00000434800.1:n.538_545delinsACTCCCCC
ENST00000532791.5:c.2321_2328delinsACTCCCCC ENSP00000432972.1:p.Tyr774=
ENST00000619564.3:c.*1222_*1229delinsACTCCCCC ENSP00000484553.1:n.*1222_*1229delinsACTCCCCC
NM_001174063.1:c.2321_2328delinsACTCCCCC NP_001167534.1:p.Tyr774=
NM_001174064.1:c.2297_2304delinsACTCCCCC NP_001167535.1:p.Tyr766=
NM_001174065.1:c.2321_2328delinsACTCCCCC NP_001167536.1:p.Tyr774=
NM_001174066.1:c.2060_2067delinsACTCCCCC NP_001167537.1:p.Tyr687=
NM_001174067.1:c.2420_2427delinsACTCCCCC NP_001167538.1:p.Tyr807=
NM_015850.3:c.2321_2328delinsACTCCCCC NP_056934.2:p.Tyr774=
NM_023105.2:c.2060_2067delinsACTCCCCC NP_075593.1:p.Tyr687=
NM_023106.2:c.2054_2061delinsACTCCCCC NP_075594.1:p.Tyr685=
NM_023110.2:c.2327_2334delinsACTCCCCC NP_075598.2:p.Tyr776=
XM_006716303.2:c.2292+148_2292+155delinsACTCCCCC XP_006716366.1:n.2292+148_2292+155delinsACTCCCCC
XM_006716304.1:c.2292+148_2292+155delinsACTCCCCC XP_006716367.1:n.2292+148_2292+155delinsACTCCCCC
XM_006716305.2:c.2292+148_2292+155delinsACTCCCCC XP_006716368.1:n.2292+148_2292+155delinsACTCCCCC
XM_006716306.2:c.2286+148_2286+155delinsACTCCCCC XP_006716369.1:n.2286+148_2286+155delinsACTCCCCC
XM_006716307.1:c.2286+148_2286+155delinsACTCCCCC XP_006716370.1:n.2286+148_2286+155delinsACTCCCCC
XM_006716309.2:c.2268+148_2268+155delinsACTCCCCC XP_006716372.1:n.2268+148_2268+155delinsACTCCCCC
XM_006716310.2:c.2025+148_2025+155delinsACTCCCCC XP_006716373.1:n.2025+148_2025+155delinsACTCCCCC
XM_006716311.1:c.2025+148_2025+155delinsACTCCCCC XP_006716374.1:n.2025+148_2025+155delinsACTCCCCC
XM_006716312.1:c.2025+148_2025+155delinsACTCCCCC XP_006716375.1:n.2025+148_2025+155delinsACTCCCCC
XM_006716313.2:c.2019+148_2019+155delinsACTCCCCC XP_006716376.1:n.2019+148_2019+155delinsACTCCCCC
XM_006716314.1:c.2019+148_2019+155delinsACTCCCCC XP_006716377.1:n.2019+148_2019+155delinsACTCCCCC
XM_011544443.1:c.2391+148_2391+155delinsACTCCCCC XP_011542745.1:n.2391+148_2391+155delinsACTCCCCC
XM_011544444.1:c.2385+148_2385+155delinsACTCCCCC XP_011542746.1:n.2385+148_2385+155delinsACTCCCCC
XM_011544445.1:c.2385+148_2385+155delinsACTCCCCC XP_011542747.1:n.2385+148_2385+155delinsACTCCCCC
XM_011544446.1:c.2426_2433delinsACTCCCCC XP_011542748.1:p.Tyr809=
XM_011544447.1:c.2420_2427delinsACTCCCCC XP_011542749.1:p.Tyr807=
XM_011544448.1:c.2124+148_2124+155delinsACTCCCCC XP_011542750.1:n.2124+148_2124+155delinsACTCCCCC
XM_011544449.1:c.2118+148_2118+155delinsACTCCCCC XP_011542751.1:n.2118+148_2118+155delinsACTCCCCC
XM_011544450.1:c.2153_2160delinsACTCCCCC XP_011542752.1:p.Tyr718=
XM_011544451.1:c.2001+148_2001+155delinsACTCCCCC XP_011542753.1:n.2001+148_2001+155delinsACTCCCCC
NM_001354367.1:c.2286+148_2286+155delinsACTCCCCC NP_001341296.1:n.2286+148_2286+155delinsACTCCCCC
NM_001354368.1:c.2048_2055delinsACTCCCCC NP_001341297.1:p.Tyr683=
NM_001354369.1:c.2280+148_2280+155delinsACTCCCCC NP_001341298.1:n.2280+148_2280+155delinsACTCCCCC
NM_001354370.1:c.2019+148_2019+155delinsACTCCCCC NP_001341299.1:n.2019+148_2019+155delinsACTCCCCC
XM_006716303.3:c.2292+148_2292+155delinsACTCCCCC XP_006716366.1:n.2292+148_2292+155delinsACTCCCCC
XM_006716310.3:c.2025+148_2025+155delinsACTCCCCC XP_006716373.1:n.2025+148_2025+155delinsACTCCCCC
XM_006716312.2:c.2025+148_2025+155delinsACTCCCCC XP_006716375.1:n.2025+148_2025+155delinsACTCCCCC
XM_006716314.2:c.2019+148_2019+155delinsACTCCCCC XP_006716377.1:n.2019+148_2019+155delinsACTCCCCC
XM_011544443.2:c.2391+148_2391+155delinsACTCCCCC XP_011542745.1:n.2391+148_2391+155delinsACTCCCCC
XM_011544445.2:c.2385+148_2385+155delinsACTCCCCC XP_011542747.1:n.2385+148_2385+155delinsACTCCCCC
XM_011544446.2:c.2426_2433delinsACTCCCCC XP_011542748.1:p.Tyr809=
XM_011544447.2:c.2420_2427delinsACTCCCCC XP_011542749.1:p.Tyr807=
XM_011544450.2:c.2153_2160delinsACTCCCCC XP_011542752.1:p.Tyr718=
XM_017013219.1:c.2379+148_2379+155delinsACTCCCCC XP_016868708.1:n.2379+148_2379+155delinsACTCCCCC
XM_017013220.1:c.2414_2421delinsACTCCCCC XP_016868709.1:p.Tyr805=
XM_017013221.1:c.2292+148_2292+155delinsACTCCCCC XP_016868710.1:n.2292+148_2292+155delinsACTCCCCC
XM_017013222.2:c.2286+148_2286+155delinsACTCCCCC XP_016868711.1:n.2286+148_2286+155delinsACTCCCCC
XM_017013224.2:c.2315_2322delinsACTCCCCC XP_016868713.1:p.Tyr772=
XM_017013225.2:c.2315_2322delinsACTCCCCC XP_016868714.1:p.Tyr772=
XM_017013226.1:c.2153_2160delinsACTCCCCC XP_016868715.1:p.Tyr718=
XM_017013227.1:c.2147_2154delinsACTCCCCC XP_016868716.1:p.Tyr716=
XM_017013229.2:c.1320+148_1320+155delinsACTCCCCC XP_016868718.1:n.1320+148_1320+155delinsACTCCCCC
XM_017013230.1:c.1355_1362delinsACTCCCCC XP_016868719.1:p.Tyr452=
XM_024447097.1:c.2268+148_2268+155delinsACTCCCCC XP_024302865.1:n.2268+148_2268+155delinsACTCCCCC
XR_001745495.1:n.2600_2607delinsACTCCCCC
XR_001745496.1:n.2565+148_2565+155delinsACTCCCCC
NM_001174063.2:c.2321_2328delinsACTCCCCC NP_001167534.1:p.Tyr774=
NM_001174064.2:c.2297_2304delinsACTCCCCC NP_001167535.1:p.Tyr766=
NM_001174065.2:c.2321_2328delinsACTCCCCC NP_001167536.1:p.Tyr774=
NM_001174066.2:c.2060_2067delinsACTCCCCC NP_001167537.1:p.Tyr687=
NM_001354368.2:c.2048_2055delinsACTCCCCC NP_001341297.1:p.Tyr683=
NM_015850.4:c.2321_2328delinsACTCCCCC NP_056934.2:p.Tyr774=
NM_023105.3:c.2060_2067delinsACTCCCCC NP_075593.1:p.Tyr687=
NM_023106.3:c.2054_2061delinsACTCCCCC NP_075594.1:p.Tyr685=
NM_023110.3:c.2327_2334delinsACTCCCCC MANE Select NP_075598.2:p.Tyr776=
NM_001174067.2:c.2420_2427delinsACTCCCCC NP_001167538.1:p.Tyr807=
NM_001354367.2:c.2286+148_2286+155delinsACTCCCCC NP_001341296.1:n.2286+148_2286+155delinsACTCCCCC
NM_001354369.2:c.2280+148_2280+155delinsACTCCCCC NP_001341298.1:n.2280+148_2280+155delinsACTCCCCC
NM_001354370.2:c.2019+148_2019+155delinsACTCCCCC NP_001341299.1:n.2019+148_2019+155delinsACTCCCCC