Canonical Allele Identifier: CA1941024621

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121517413C= , CM000672.2:g.121517413C=	GRCh38
NC_000010.10:g.123276927C= , CM000672.1:g.123276927C=	GRCh37
NC_000010.9:g.123266917C=	NCBI36
NG_012449.1:g.86046G=
NG_012449.2:g.86046G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1087+1269G= MANE Plus Clinical	ENSP00000410294.2:n.1087+1269G=
ENST00000351936.11:c.990G=	ENSP00000309878.10:p.Arg330=
ENST00000638709.2:c.-181G=	ENSP00000491912.2:n.-181G=
ENST00000682296.1:n.338G=
ENST00000682400.1:n.645G=
ENST00000682550.1:c.645G=	ENSP00000507633.1:p.Arg215=
ENST00000682772.1:c.-181G=	ENSP00000506848.1:n.-181G=
ENST00000683211.1:c.990G=	ENSP00000508257.1:p.Arg330=
ENST00000683250.1:c.404-13472G=	ENSP00000506847.1:n.404-13472G=
ENST00000683418.1:n.3337G=
ENST00000683678.1:n.990G=
ENST00000684153.1:c.645G=	ENSP00000506937.1:p.Arg215=
ENST00000358487.10:c.990G= MANE Select	ENSP00000351276.6:p.Arg330=
ENST00000336553.10:c.723G=	ENSP00000337665.6:p.Arg241=
ENST00000346997.6:c.990G=	ENSP00000263451.5:p.Arg330=
ENST00000351936.10:c.996G=	ENSP00000309878.9:p.Arg332=
ENST00000356226.8:c.645G=	ENSP00000348559.4:p.Arg215=
ENST00000357555.9:c.723G=	ENSP00000350166.5:p.Arg241=
ENST00000358487.9:c.990G=	ENSP00000351276.5:p.Arg330=
ENST00000360144.7:c.820+1269G=	ENSP00000353262.3:n.820+1269G=
ENST00000369056.5:c.1087+1269G=	ENSP00000358052.1:n.1087+1269G=
ENST00000369058.7:c.1087+1269G=	ENSP00000358054.3:n.1087+1269G=
ENST00000369059.5:c.742+1269G=	ENSP00000358055.1:n.742+1269G=
ENST00000369060.8:c.939+2566G=	ENSP00000358056.4:n.939+2566G=
ENST00000369061.8:c.749-2094G=	ENSP00000358057.4:n.749-2094G=
ENST00000457416.6:c.1087+1269G=	ENSP00000410294.2:n.1087+1269G=
ENST00000463870.5:n.199G=
ENST00000478859.5:c.306G=	ENSP00000474011.1:p.Arg102=
ENST00000490349.5:n.1399G=
ENST00000604236.5:c.*37G=	ENSP00000474109.1:n.*37G=
ENST00000613048.4:c.723G=	ENSP00000484154.1:p.Arg241=
NM_000141.4:c.990G=	NP_000132.3:p.Arg330=
NM_001144913.1:c.1087+1269G=	NP_001138385.1:n.1087+1269G=
NM_001144914.1:c.749-2094G=	NP_001138386.1:n.749-2094G=
NM_001144915.1:c.723G=	NP_001138387.1:p.Arg241=
NM_001144916.1:c.645G=	NP_001138388.1:p.Arg215=
NM_001144917.1:c.939+2566G=	NP_001138389.1:n.939+2566G=
NM_001144918.1:c.645G=	NP_001138390.1:p.Arg215=
NM_001144919.1:c.820+1269G=	NP_001138391.1:n.820+1269G=
NM_022970.3:c.1087+1269G=	NP_075259.4:n.1087+1269G=
NM_023029.2:c.723G=	NP_075418.1:p.Arg241=
NR_073009.1:n.1440G=
XM_006717708.2:c.1144+1269G=	XP_006717771.1:n.1144+1269G=
XM_006717709.2:c.1047G=	XP_006717772.1:p.Arg349=
XM_006717710.2:c.1144+1269G=	XP_006717773.1:n.1144+1269G=
XM_006717711.2:c.877+1269G=	XP_006717774.1:n.877+1269G=
XM_006717712.2:c.799+1269G=	XP_006717775.1:n.799+1269G=
XM_006717713.2:c.1047G=	XP_006717776.1:p.Arg349=
XM_011539510.1:c.306G=	XP_011537812.1:p.Arg102=
NM_001320654.1:c.306G=	NP_001307583.1:p.Arg102=
NM_001320658.1:c.990G=	NP_001307587.1:p.Arg330=
XM_006717708.3:c.1144+1269G=	XP_006717771.1:n.1144+1269G=
XM_006717710.4:c.1144+1269G=	XP_006717773.1:n.1144+1269G=
XM_017015920.2:c.1144+1269G=	XP_016871409.1:n.1144+1269G=
XM_017015921.2:c.1047G=	XP_016871410.1:p.Arg349=
XM_017015924.2:c.702G=	XP_016871413.1:p.Arg234=
XM_017015925.2:c.702G=	XP_016871414.1:p.Arg234=
XM_024447887.1:c.780G=	XP_024303655.1:p.Arg260=
XM_024447888.1:c.877+1269G=	XP_024303656.1:n.877+1269G=
XM_024447889.1:c.780G=	XP_024303657.1:p.Arg260=
XM_024447890.1:c.877+1269G=	XP_024303658.1:n.877+1269G=
XM_024447891.1:c.799+1269G=	XP_024303659.1:n.799+1269G=
XM_024447892.1:c.-181G=	XP_024303660.1:n.-181G=
NM_000141.5:c.990G= MANE Select	NP_000132.3:p.Arg330=
NM_001144917.2:c.939+2566G=	NP_001138389.1:n.939+2566G=
NM_001144918.2:c.645G=	NP_001138390.1:p.Arg215=
NM_001144919.2:c.820+1269G=	NP_001138391.1:n.820+1269G=
NM_001320658.2:c.990G=	NP_001307587.1:p.Arg330=
NR_073009.2:n.1426G=
NM_001144915.2:c.723G=	NP_001138387.1:p.Arg241=
NM_001144916.2:c.645G=	NP_001138388.1:p.Arg215=
NM_001320654.2:c.306G=	NP_001307583.1:p.Arg102=