Canonical Allele Identifier: CA1941023673

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515125G= , CM000672.2:g.121515125G=	GRCh38
NC_000010.10:g.123274639G= , CM000672.1:g.123274639G=	GRCh37
NC_000010.9:g.123264629G=	NCBI36
NG_012449.1:g.88334C=
NG_012449.2:g.88334C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1282C= MANE Plus Clinical	ENSP00000410294.2:p.Gln428=
ENST00000351936.11:c.1279C=	ENSP00000309878.10:p.Gln427=
ENST00000638709.2:c.109C=	ENSP00000491912.2:p.Gln37=
ENST00000682296.1:n.627C=
ENST00000682550.1:c.934C=	ENSP00000507633.1:p.Gln312=
ENST00000682772.1:c.109C=	ENSP00000506848.1:p.Gln37=
ENST00000683211.1:c.1279C=	ENSP00000508257.1:p.Gln427=
ENST00000683250.1:c.404-11184C=	ENSP00000506847.1:n.404-11184C=
ENST00000683418.1:n.3626C=
ENST00000684153.1:c.934C=	ENSP00000506937.1:p.Gln312=
ENST00000358487.10:c.1279C= MANE Select	ENSP00000351276.6:p.Gln427=
ENST00000336553.10:c.1012C=	ENSP00000337665.6:p.Gln338=
ENST00000346997.6:c.1279C=	ENSP00000263451.5:p.Gln427=
ENST00000351936.10:c.1285C=	ENSP00000309878.9:p.Gln429=
ENST00000356226.8:c.934C=	ENSP00000348559.4:p.Gln312=
ENST00000357555.9:c.1012C=	ENSP00000350166.5:p.Gln338=
ENST00000358487.9:c.1279C=	ENSP00000351276.5:p.Gln427=
ENST00000360144.7:c.1015C=	ENSP00000353262.3:p.Gln339=
ENST00000369056.5:c.1282C=	ENSP00000358052.1:p.Gln428=
ENST00000369058.7:c.1282C=	ENSP00000358054.3:p.Gln428=
ENST00000369059.5:c.937C=	ENSP00000358055.1:p.Gln313=
ENST00000369060.8:c.939+4854C=	ENSP00000358056.4:n.939+4854C=
ENST00000369061.8:c.943C=	ENSP00000358057.4:p.Gln315=
ENST00000429361.5:c.55C=	ENSP00000404219.1:p.Gln19=
ENST00000457416.6:c.1282C=	ENSP00000410294.2:p.Gln428=
ENST00000478859.5:c.595C=	ENSP00000474011.1:p.Gln199=
ENST00000604236.5:c.*326C=	ENSP00000474109.1:n.*326C=
ENST00000613048.4:c.1012C=	ENSP00000484154.1:p.Gln338=
NM_000141.4:c.1279C=	NP_000132.3:p.Gln427=
NM_001144913.1:c.1282C=	NP_001138385.1:p.Gln428=
NM_001144914.1:c.943C=	NP_001138386.1:p.Gln315=
NM_001144915.1:c.1012C=	NP_001138387.1:p.Gln338=
NM_001144916.1:c.934C=	NP_001138388.1:p.Gln312=
NM_001144917.1:c.939+4854C=	NP_001138389.1:n.939+4854C=
NM_001144918.1:c.934C=	NP_001138390.1:p.Gln312=
NM_001144919.1:c.1015C=	NP_001138391.1:p.Gln339=
NM_022970.3:c.1282C=	NP_075259.4:p.Gln428=
NM_023029.2:c.1012C=	NP_075418.1:p.Gln338=
NR_073009.1:n.1729C=
XM_006717708.2:c.1339C=	XP_006717771.1:p.Gln447=
XM_006717709.2:c.1336C=	XP_006717772.1:p.Gln446=
XM_006717710.2:c.1339C=	XP_006717773.1:p.Gln447=
XM_006717711.2:c.1072C=	XP_006717774.1:p.Gln358=
XM_006717712.2:c.994C=	XP_006717775.1:p.Gln332=
XM_006717713.2:c.1336C=	XP_006717776.1:p.Gln446=
XM_011539510.1:c.595C=	XP_011537812.1:p.Gln199=
NM_001320654.1:c.595C=	NP_001307583.1:p.Gln199=
NM_001320658.1:c.1279C=	NP_001307587.1:p.Gln427=
XM_006717708.3:c.1339C=	XP_006717771.1:p.Gln447=
XM_006717710.4:c.1339C=	XP_006717773.1:p.Gln447=
XM_017015920.2:c.1339C=	XP_016871409.1:p.Gln447=
XM_017015921.2:c.1336C=	XP_016871410.1:p.Gln446=
XM_017015924.2:c.991C=	XP_016871413.1:p.Gln331=
XM_017015925.2:c.991C=	XP_016871414.1:p.Gln331=
XM_024447887.1:c.1069C=	XP_024303655.1:p.Gln357=
XM_024447888.1:c.1072C=	XP_024303656.1:p.Gln358=
XM_024447889.1:c.1069C=	XP_024303657.1:p.Gln357=
XM_024447890.1:c.1072C=	XP_024303658.1:p.Gln358=
XM_024447891.1:c.994C=	XP_024303659.1:p.Gln332=
XM_024447892.1:c.109C=	XP_024303660.1:p.Gln37=
NM_000141.5:c.1279C= MANE Select	NP_000132.3:p.Gln427=
NM_001144917.2:c.939+4854C=	NP_001138389.1:n.939+4854C=
NM_001144918.2:c.934C=	NP_001138390.1:p.Gln312=
NM_001144919.2:c.1015C=	NP_001138391.1:p.Gln339=
NM_001320658.2:c.1279C=	NP_001307587.1:p.Gln427=
NR_073009.2:n.1715C=
NM_001144915.2:c.1012C=	NP_001138387.1:p.Gln338=
NM_001144916.2:c.934C=	NP_001138388.1:p.Gln312=
NM_001320654.2:c.595C=	NP_001307583.1:p.Gln199=