Canonical Allele Identifier: CA1941012769

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488093T= , CM000672.2:g.121488093T=	GRCh38
NC_000010.10:g.123247607T= , CM000672.1:g.123247607T=	GRCh37
NC_000010.9:g.123237597T=	NCBI36
NG_012449.1:g.115366A=
NG_012449.2:g.115366A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1887A= MANE Plus Clinical	ENSP00000410294.2:p.Ala629=
ENST00000351936.11:c.1878A=	ENSP00000309878.10:p.Ala626=
ENST00000638709.2:c.708A=	ENSP00000491912.2:p.Ala236=
ENST00000682296.1:n.1226A=
ENST00000682550.1:c.1533A=	ENSP00000507633.1:p.Ala511=
ENST00000682772.1:c.708A=	ENSP00000506848.1:p.Ala236=
ENST00000682904.1:n.704A=
ENST00000683029.1:n.296A=
ENST00000683211.1:c.1878A=	ENSP00000508257.1:p.Ala626=
ENST00000683250.1:c.*586A=	ENSP00000506847.1:n.*586A=
ENST00000683418.1:n.4225A=
ENST00000684153.1:c.1533A=	ENSP00000506937.1:p.Ala511=
ENST00000684516.1:n.2897A=
ENST00000358487.10:c.1884A= MANE Select	ENSP00000351276.6:p.Ala628=
ENST00000336553.10:c.1611A=	ENSP00000337665.6:p.Ala537=
ENST00000346997.6:c.1878A=	ENSP00000263451.5:p.Ala626=
ENST00000351936.10:c.1884A=	ENSP00000309878.9:p.Ala628=
ENST00000356226.8:c.1533A=	ENSP00000348559.4:p.Ala511=
ENST00000357555.9:c.1617A=	ENSP00000350166.5:p.Ala539=
ENST00000358487.9:c.1884A=	ENSP00000351276.5:p.Ala628=
ENST00000360144.7:c.1620A=	ENSP00000353262.3:p.Ala540=
ENST00000369056.5:c.1887A=	ENSP00000358052.1:p.Ala629=
ENST00000369058.7:c.1887A=	ENSP00000358054.3:p.Ala629=
ENST00000369059.5:c.1542A=	ENSP00000358055.1:p.Ala514=
ENST00000369060.8:c.1536A=	ENSP00000358056.4:p.Ala512=
ENST00000369061.8:c.1548A=	ENSP00000358057.4:p.Ala516=
ENST00000429361.5:c.660A=	ENSP00000404219.1:p.Ala220=
ENST00000457416.6:c.1887A=	ENSP00000410294.2:p.Ala629=
ENST00000478859.5:c.1200A=	ENSP00000474011.1:p.Ala400=
ENST00000604236.5:c.*931A=	ENSP00000474109.1:n.*931A=
ENST00000613048.4:c.1617A=	ENSP00000484154.1:p.Ala539=
NM_000141.4:c.1884A=	NP_000132.3:p.Ala628=
NM_001144913.1:c.1887A=	NP_001138385.1:p.Ala629=
NM_001144914.1:c.1548A=	NP_001138386.1:p.Ala516=
NM_001144915.1:c.1617A=	NP_001138387.1:p.Ala539=
NM_001144916.1:c.1539A=	NP_001138388.1:p.Ala513=
NM_001144917.1:c.1536A=	NP_001138389.1:p.Ala512=
NM_001144918.1:c.1533A=	NP_001138390.1:p.Ala511=
NM_001144919.1:c.1620A=	NP_001138391.1:p.Ala540=
NM_022970.3:c.1887A=	NP_075259.4:p.Ala629=
NM_023029.2:c.1617A=	NP_075418.1:p.Ala539=
NR_073009.1:n.2334A=
XM_006717708.2:c.1938A=	XP_006717771.1:p.Ala646=
XM_006717709.2:c.1935A=	XP_006717772.1:p.Ala645=
XM_006717710.2:c.1944A=	XP_006717773.1:p.Ala648=
XM_006717711.2:c.1677A=	XP_006717774.1:p.Ala559=
XM_006717712.2:c.1599A=	XP_006717775.1:p.Ala533=
XM_006717713.2:c.1941A=	XP_006717776.1:p.Ala647=
XM_011539510.1:c.1200A=	XP_011537812.1:p.Ala400=
NM_001320654.1:c.1200A=	NP_001307583.1:p.Ala400=
NM_001320658.1:c.1878A=	NP_001307587.1:p.Ala626=
XM_006717708.3:c.1938A=	XP_006717771.1:p.Ala646=
XM_006717710.4:c.1944A=	XP_006717773.1:p.Ala648=
XM_017015920.2:c.1938A=	XP_016871409.1:p.Ala646=
XM_017015921.2:c.1935A=	XP_016871410.1:p.Ala645=
XM_017015924.2:c.1596A=	XP_016871413.1:p.Ala532=
XM_017015925.2:c.1590A=	XP_016871414.1:p.Ala530=
XM_024447887.1:c.1674A=	XP_024303655.1:p.Ala558=
XM_024447888.1:c.1671A=	XP_024303656.1:p.Ala557=
XM_024447889.1:c.1668A=	XP_024303657.1:p.Ala556=
XM_024447890.1:c.1677A=	XP_024303658.1:p.Ala559=
XM_024447891.1:c.1599A=	XP_024303659.1:p.Ala533=
XM_024447892.1:c.714A=	XP_024303660.1:p.Ala238=
NM_000141.5:c.1884A= MANE Select	NP_000132.3:p.Ala628=
NM_001144917.2:c.1536A=	NP_001138389.1:p.Ala512=
NM_001144918.2:c.1533A=	NP_001138390.1:p.Ala511=
NM_001144919.2:c.1620A=	NP_001138391.1:p.Ala540=
NM_001320658.2:c.1878A=	NP_001307587.1:p.Ala626=
NR_073009.2:n.2320A=
NM_001144915.2:c.1617A=	NP_001138387.1:p.Ala539=
NM_001144916.2:c.1539A=	NP_001138388.1:p.Ala513=
NM_001320654.2:c.1200A=	NP_001307583.1:p.Ala400=