Canonical Allele Identifier: CA370728517

Gene: FGFR1

Linked Data

• ClinVar Variation Id: 2505453
• ClinVar RCV Id: RCV003234721
• dbSNP Id: rs1057520536
• MyVariant Identifiers: chr8:g.38271704G>A (hg19) ; chr8:g.38414186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38414186G>A , CM000670.2:g.38414186G>A	GRCh38
NC_000008.10:g.38271704G>A , CM000670.1:g.38271704G>A	GRCh37
NC_000008.9:g.38390861G>A	NCBI36
NG_007729.1:g.59649C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000703405.1:c.2152C>T	ENSP00000515291.1:p.Arg718Cys
ENST00000341462.9:c.2140C>T	ENSP00000340636.7:p.Arg714Cys
ENST00000425967.8:c.2140C>T	ENSP00000393312.4:p.Arg714Cys
ENST00000524528.2:n.3045C>T
ENST00000682398.1:n.1392C>T
ENST00000683132.1:n.842C>T
ENST00000683765.1:c.2332C>T	ENSP00000507039.1:p.Arg778Cys
ENST00000683815.1:c.2140C>T	ENSP00000507997.1:p.Arg714Cys
ENST00000683948.1:n.2840C>T
ENST00000684654.1:c.1873C>T	ENSP00000507205.1:p.Arg625Cys
ENST00000447712.7:c.2152C>T MANE Select	ENSP00000400162.2:p.Arg718Cys
ENST00000649678.1:c.2140C>T	ENSP00000497266.1:p.Arg714Cys
ENST00000674189.1:c.*1798C>T	ENSP00000501345.1:n.*1798C>T
ENST00000674380.1:c.*2119C>T	ENSP00000501514.1:n.*2119C>T
ENST00000674474.1:n.3646C>T
ENST00000326324.10:c.1879C>T	ENSP00000327229.6:p.Arg627Cys
ENST00000335922.9:c.2122C>T	ENSP00000337247.5:p.Arg708Cys
ENST00000341462.8:c.*1202C>T	ENSP00000340636.6:n.*1202C>T
ENST00000356207.9:c.1885C>T	ENSP00000348537.5:p.Arg629Cys
ENST00000397091.9:c.2146C>T	ENSP00000380280.5:p.Arg716Cys
ENST00000397103.5:c.1885C>T	ENSP00000380292.1:p.Arg629Cys
ENST00000397108.8:c.2146C>T	ENSP00000380297.4:p.Arg716Cys
ENST00000397113.6:c.2146C>T	ENSP00000380302.2:p.Arg716Cys
ENST00000425967.7:c.2245C>T	ENSP00000393312.3:p.Arg749Cys
ENST00000447712.6:c.2152C>T	ENSP00000400162.2:p.Arg718Cys
ENST00000526570.5:n.4431C>T
ENST00000531196.5:c.352C>T	ENSP00000434800.1:p.Arg118Cys
ENST00000532791.5:c.2146C>T	ENSP00000432972.1:p.Arg716Cys
ENST00000619564.3:c.*1047C>T	ENSP00000484553.1:n.*1047C>T
NM_001174063.1:c.2146C>T	NP_001167534.1:p.Arg716Cys
NM_001174064.1:c.2122C>T	NP_001167535.1:p.Arg708Cys
NM_001174065.1:c.2146C>T	NP_001167536.1:p.Arg716Cys
NM_001174066.1:c.1885C>T	NP_001167537.1:p.Arg629Cys
NM_001174067.1:c.2245C>T	NP_001167538.1:p.Arg749Cys
NM_015850.3:c.2146C>T	NP_056934.2:p.Arg716Cys
NM_023105.2:c.1885C>T	NP_075593.1:p.Arg629Cys
NM_023106.2:c.1879C>T	NP_075594.1:p.Arg627Cys
NM_023110.2:c.2152C>T	NP_075598.2:p.Arg718Cys
XM_006716303.2:c.2152C>T	XP_006716366.1:p.Arg718Cys
XM_006716304.1:c.2152C>T	XP_006716367.1:p.Arg718Cys
XM_006716305.2:c.2152C>T	XP_006716368.1:p.Arg718Cys
XM_006716306.2:c.2146C>T	XP_006716369.1:p.Arg716Cys
XM_006716307.1:c.2146C>T	XP_006716370.1:p.Arg716Cys
XM_006716309.2:c.2128C>T	XP_006716372.1:p.Arg710Cys
XM_006716310.2:c.1885C>T	XP_006716373.1:p.Arg629Cys
XM_006716311.1:c.1885C>T	XP_006716374.1:p.Arg629Cys
XM_006716312.1:c.1885C>T	XP_006716375.1:p.Arg629Cys
XM_006716313.2:c.1879C>T	XP_006716376.1:p.Arg627Cys
XM_006716314.1:c.1879C>T	XP_006716377.1:p.Arg627Cys
XM_011544443.1:c.2251C>T	XP_011542745.1:p.Arg751Cys
XM_011544444.1:c.2245C>T	XP_011542746.1:p.Arg749Cys
XM_011544445.1:c.2245C>T	XP_011542747.1:p.Arg749Cys
XM_011544446.1:c.2251C>T	XP_011542748.1:p.Arg751Cys
XM_011544447.1:c.2245C>T	XP_011542749.1:p.Arg749Cys
XM_011544448.1:c.1984C>T	XP_011542750.1:p.Arg662Cys
XM_011544449.1:c.1978C>T	XP_011542751.1:p.Arg660Cys
XM_011544450.1:c.1978C>T	XP_011542752.1:p.Arg660Cys
XM_011544451.1:c.1861C>T	XP_011542753.1:p.Arg621Cys
NM_001354367.1:c.2146C>T	NP_001341296.1:p.Arg716Cys
NM_001354368.1:c.1873C>T	NP_001341297.1:p.Arg625Cys
NM_001354369.1:c.2140C>T	NP_001341298.1:p.Arg714Cys
NM_001354370.1:c.1879C>T	NP_001341299.1:p.Arg627Cys
XM_006716303.3:c.2152C>T	XP_006716366.1:p.Arg718Cys
XM_006716310.3:c.1885C>T	XP_006716373.1:p.Arg629Cys
XM_006716312.2:c.1885C>T	XP_006716375.1:p.Arg629Cys
XM_006716314.2:c.1879C>T	XP_006716377.1:p.Arg627Cys
XM_011544443.2:c.2251C>T	XP_011542745.1:p.Arg751Cys
XM_011544445.2:c.2245C>T	XP_011542747.1:p.Arg749Cys
XM_011544446.2:c.2251C>T	XP_011542748.1:p.Arg751Cys
XM_011544447.2:c.2245C>T	XP_011542749.1:p.Arg749Cys
XM_011544450.2:c.1978C>T	XP_011542752.1:p.Arg660Cys
XM_017013219.1:c.2239C>T	XP_016868708.1:p.Arg747Cys
XM_017013220.1:c.2239C>T	XP_016868709.1:p.Arg747Cys
XM_017013221.1:c.2152C>T	XP_016868710.1:p.Arg718Cys
XM_017013222.2:c.2146C>T	XP_016868711.1:p.Arg716Cys
XM_017013224.2:c.2140C>T	XP_016868713.1:p.Arg714Cys
XM_017013225.2:c.2140C>T	XP_016868714.1:p.Arg714Cys
XM_017013226.1:c.1978C>T	XP_016868715.1:p.Arg660Cys
XM_017013227.1:c.1972C>T	XP_016868716.1:p.Arg658Cys
XM_017013229.2:c.1180C>T	XP_016868718.1:p.Arg394Cys
XM_017013230.1:c.1180C>T	XP_016868719.1:p.Arg394Cys
XM_024447097.1:c.2128C>T	XP_024302865.1:p.Arg710Cys
XR_001745495.1:n.2425C>T
XR_001745496.1:n.2425C>T
NM_001174063.2:c.2146C>T	NP_001167534.1:p.Arg716Cys
NM_001174064.2:c.2122C>T	NP_001167535.1:p.Arg708Cys
NM_001174065.2:c.2146C>T	NP_001167536.1:p.Arg716Cys
NM_001174066.2:c.1885C>T	NP_001167537.1:p.Arg629Cys
NM_001354368.2:c.1873C>T	NP_001341297.1:p.Arg625Cys
NM_015850.4:c.2146C>T	NP_056934.2:p.Arg716Cys
NM_023105.3:c.1885C>T	NP_075593.1:p.Arg629Cys
NM_023106.3:c.1879C>T	NP_075594.1:p.Arg627Cys
NM_023110.3:c.2152C>T MANE Select	NP_075598.2:p.Arg718Cys
NM_001174067.2:c.2245C>T	NP_001167538.1:p.Arg749Cys
NM_001354367.2:c.2146C>T	NP_001341296.1:p.Arg716Cys
NM_001354369.2:c.2140C>T	NP_001341298.1:p.Arg714Cys
NM_001354370.2:c.1879C>T	NP_001341299.1:p.Arg627Cys