Canonical Allele Identifier: CA1777533116

Gene: FGFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38413725_38413727delinsCCT , CM000670.2:g.38413725_38413727delinsCCT	GRCh38
NC_000008.10:g.38271243_38271245delinsCCT , CM000670.1:g.38271243_38271245delinsCCT	GRCh37
NC_000008.9:g.38390400_38390402delinsCCT	NCBI36
NG_007729.1:g.60108_60110delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703405.1:c.2370_2372delinsAGG	ENSP00000515291.1:p.Ser790=
ENST00000341462.9:c.2280+191_2280+193delinsAGG	ENSP00000340636.7:n.2280+191_2280+193delinsAGG
ENST00000425967.8:c.2280+191_2280+193delinsAGG	ENSP00000393312.4:n.2280+191_2280+193delinsAGG
ENST00000524528.2:n.3263_3265delinsAGG
ENST00000682398.1:n.1610_1612delinsAGG
ENST00000683132.1:n.1173_1175delinsAGG
ENST00000683765.1:c.2472+191_2472+193delinsAGG	ENSP00000507039.1:n.2472+191_2472+193delinsAGG
ENST00000683815.1:c.2358_2360delinsAGG	ENSP00000507997.1:p.Ser786=
ENST00000683948.1:n.3058_3060delinsAGG
ENST00000684654.1:c.2091_2093delinsAGG	ENSP00000507205.1:p.Ser697=
ENST00000447712.7:c.2370_2372delinsAGG MANE Select	ENSP00000400162.2:p.Ser790=
ENST00000649678.1:c.2358_2360delinsAGG	ENSP00000497266.1:p.Ser786=
ENST00000674189.1:c.*1938+191_*1938+193delinsAGG	ENSP00000501345.1:n.*1938+191_*1938+193delinsAGG
ENST00000674380.1:c.*2337_*2339delinsAGG	ENSP00000501514.1:n.*2337_*2339delinsAGG
ENST00000674474.1:n.3864_3866delinsAGG
ENST00000326324.10:c.2097_2099delinsAGG	ENSP00000327229.6:p.Ser699=
ENST00000335922.9:c.2340_2342delinsAGG	ENSP00000337247.5:p.Ser780=
ENST00000341462.8:c.*1420_*1422delinsAGG	ENSP00000340636.6:n.*1420_*1422delinsAGG
ENST00000356207.9:c.2103_2105delinsAGG	ENSP00000348537.5:p.Ser701=
ENST00000397091.9:c.2364_2366delinsAGG	ENSP00000380280.5:p.Ser788=
ENST00000397103.5:c.2103_2105delinsAGG	ENSP00000380292.1:p.Ser701=
ENST00000397108.8:c.2364_2366delinsAGG	ENSP00000380297.4:p.Ser788=
ENST00000397113.6:c.2364_2366delinsAGG	ENSP00000380302.2:p.Ser788=
ENST00000425967.7:c.2463_2465delinsAGG	ENSP00000393312.3:p.Ser821=
ENST00000447712.6:c.2370_2372delinsAGG	ENSP00000400162.2:p.Ser790=
ENST00000526570.5:n.4649_4651delinsAGG
ENST00000526688.1:n.59+191_59+193delinsAGG
ENST00000531196.5:c.581_583delinsAGG	ENSP00000434800.1:n.581_583delinsAGG
ENST00000532791.5:c.2364_2366delinsAGG	ENSP00000432972.1:p.Ser788=
ENST00000619564.3:c.*1265_*1267delinsAGG	ENSP00000484553.1:n.*1265_*1267delinsAGG
NM_001174063.1:c.2364_2366delinsAGG	NP_001167534.1:p.Ser788=
NM_001174064.1:c.2340_2342delinsAGG	NP_001167535.1:p.Ser780=
NM_001174065.1:c.2364_2366delinsAGG	NP_001167536.1:p.Ser788=
NM_001174066.1:c.2103_2105delinsAGG	NP_001167537.1:p.Ser701=
NM_001174067.1:c.2463_2465delinsAGG	NP_001167538.1:p.Ser821=
NM_015850.3:c.2364_2366delinsAGG	NP_056934.2:p.Ser788=
NM_023105.2:c.2103_2105delinsAGG	NP_075593.1:p.Ser701=
NM_023106.2:c.2097_2099delinsAGG	NP_075594.1:p.Ser699=
NM_023110.2:c.2370_2372delinsAGG	NP_075598.2:p.Ser790=
XM_006716303.2:c.2292+191_2292+193delinsAGG	XP_006716366.1:n.2292+191_2292+193delinsAGG
XM_006716304.1:c.2292+191_2292+193delinsAGG	XP_006716367.1:n.2292+191_2292+193delinsAGG
XM_006716305.2:c.2292+191_2292+193delinsAGG	XP_006716368.1:n.2292+191_2292+193delinsAGG
XM_006716306.2:c.2286+191_2286+193delinsAGG	XP_006716369.1:n.2286+191_2286+193delinsAGG
XM_006716307.1:c.2286+191_2286+193delinsAGG	XP_006716370.1:n.2286+191_2286+193delinsAGG
XM_006716309.2:c.2268+191_2268+193delinsAGG	XP_006716372.1:n.2268+191_2268+193delinsAGG
XM_006716310.2:c.2025+191_2025+193delinsAGG	XP_006716373.1:n.2025+191_2025+193delinsAGG
XM_006716311.1:c.2025+191_2025+193delinsAGG	XP_006716374.1:n.2025+191_2025+193delinsAGG
XM_006716312.1:c.2025+191_2025+193delinsAGG	XP_006716375.1:n.2025+191_2025+193delinsAGG
XM_006716313.2:c.2019+191_2019+193delinsAGG	XP_006716376.1:n.2019+191_2019+193delinsAGG
XM_006716314.1:c.2019+191_2019+193delinsAGG	XP_006716377.1:n.2019+191_2019+193delinsAGG
XM_011544443.1:c.2391+191_2391+193delinsAGG	XP_011542745.1:n.2391+191_2391+193delinsAGG
XM_011544444.1:c.2385+191_2385+193delinsAGG	XP_011542746.1:n.2385+191_2385+193delinsAGG
XM_011544445.1:c.2385+191_2385+193delinsAGG	XP_011542747.1:n.2385+191_2385+193delinsAGG
XM_011544446.1:c.2469_2471delinsAGG	XP_011542748.1:p.Ser823=
XM_011544447.1:c.2463_2465delinsAGG	XP_011542749.1:p.Ser821=
XM_011544448.1:c.2124+191_2124+193delinsAGG	XP_011542750.1:n.2124+191_2124+193delinsAGG
XM_011544449.1:c.2118+191_2118+193delinsAGG	XP_011542751.1:n.2118+191_2118+193delinsAGG
XM_011544450.1:c.2196_2198delinsAGG	XP_011542752.1:p.Ser732=
XM_011544451.1:c.2001+191_2001+193delinsAGG	XP_011542753.1:n.2001+191_2001+193delinsAGG
NM_001354367.1:c.2286+191_2286+193delinsAGG	NP_001341296.1:n.2286+191_2286+193delinsAGG
NM_001354368.1:c.2091_2093delinsAGG	NP_001341297.1:p.Ser697=
NM_001354369.1:c.2280+191_2280+193delinsAGG	NP_001341298.1:n.2280+191_2280+193delinsAGG
NM_001354370.1:c.2019+191_2019+193delinsAGG	NP_001341299.1:n.2019+191_2019+193delinsAGG
XM_006716303.3:c.2292+191_2292+193delinsAGG	XP_006716366.1:n.2292+191_2292+193delinsAGG
XM_006716310.3:c.2025+191_2025+193delinsAGG	XP_006716373.1:n.2025+191_2025+193delinsAGG
XM_006716312.2:c.2025+191_2025+193delinsAGG	XP_006716375.1:n.2025+191_2025+193delinsAGG
XM_006716314.2:c.2019+191_2019+193delinsAGG	XP_006716377.1:n.2019+191_2019+193delinsAGG
XM_011544443.2:c.2391+191_2391+193delinsAGG	XP_011542745.1:n.2391+191_2391+193delinsAGG
XM_011544445.2:c.2385+191_2385+193delinsAGG	XP_011542747.1:n.2385+191_2385+193delinsAGG
XM_011544446.2:c.2469_2471delinsAGG	XP_011542748.1:p.Ser823=
XM_011544447.2:c.2463_2465delinsAGG	XP_011542749.1:p.Ser821=
XM_011544450.2:c.2196_2198delinsAGG	XP_011542752.1:p.Ser732=
XM_017013219.1:c.2379+191_2379+193delinsAGG	XP_016868708.1:n.2379+191_2379+193delinsAGG
XM_017013220.1:c.2457_2459delinsAGG	XP_016868709.1:p.Ser819=
XM_017013221.1:c.2292+191_2292+193delinsAGG	XP_016868710.1:n.2292+191_2292+193delinsAGG
XM_017013222.2:c.2286+191_2286+193delinsAGG	XP_016868711.1:n.2286+191_2286+193delinsAGG
XM_017013224.2:c.2358_2360delinsAGG	XP_016868713.1:p.Ser786=
XM_017013225.2:c.2358_2360delinsAGG	XP_016868714.1:p.Ser786=
XM_017013226.1:c.2196_2198delinsAGG	XP_016868715.1:p.Ser732=
XM_017013227.1:c.2190_2192delinsAGG	XP_016868716.1:p.Ser730=
XM_017013229.2:c.1320+191_1320+193delinsAGG	XP_016868718.1:n.1320+191_1320+193delinsAGG
XM_017013230.1:c.1398_1400delinsAGG	XP_016868719.1:p.Ser466=
XM_024447097.1:c.2268+191_2268+193delinsAGG	XP_024302865.1:n.2268+191_2268+193delinsAGG
XR_001745495.1:n.2643_2645delinsAGG
XR_001745496.1:n.2565+191_2565+193delinsAGG
NM_001174063.2:c.2364_2366delinsAGG	NP_001167534.1:p.Ser788=
NM_001174064.2:c.2340_2342delinsAGG	NP_001167535.1:p.Ser780=
NM_001174065.2:c.2364_2366delinsAGG	NP_001167536.1:p.Ser788=
NM_001174066.2:c.2103_2105delinsAGG	NP_001167537.1:p.Ser701=
NM_001354368.2:c.2091_2093delinsAGG	NP_001341297.1:p.Ser697=
NM_015850.4:c.2364_2366delinsAGG	NP_056934.2:p.Ser788=
NM_023105.3:c.2103_2105delinsAGG	NP_075593.1:p.Ser701=
NM_023106.3:c.2097_2099delinsAGG	NP_075594.1:p.Ser699=
NM_023110.3:c.2370_2372delinsAGG MANE Select	NP_075598.2:p.Ser790=
NM_001174067.2:c.2463_2465delinsAGG	NP_001167538.1:p.Ser821=
NM_001354367.2:c.2286+191_2286+193delinsAGG	NP_001341296.1:n.2286+191_2286+193delinsAGG
NM_001354369.2:c.2280+191_2280+193delinsAGG	NP_001341298.1:n.2280+191_2280+193delinsAGG
NM_001354370.2:c.2019+191_2019+193delinsAGG	NP_001341299.1:n.2019+191_2019+193delinsAGG