Canonical Allele Identifier: CA1941012743

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488015T= , CM000672.2:g.121488015T=	GRCh38
NC_000010.10:g.123247529T= , CM000672.1:g.123247529T=	GRCh37
NC_000010.9:g.123237519T=	NCBI36
NG_012449.1:g.115444A=
NG_012449.2:g.115444A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1965A= MANE Plus Clinical	ENSP00000410294.2:p.Ile655=
ENST00000351936.11:c.1956A=	ENSP00000309878.10:p.Ile652=
ENST00000638709.2:c.786A=	ENSP00000491912.2:p.Ile262=
ENST00000682296.1:n.1304A=
ENST00000682550.1:c.1611A=	ENSP00000507633.1:p.Ile537=
ENST00000682772.1:c.786A=	ENSP00000506848.1:p.Ile262=
ENST00000682904.1:n.782A=
ENST00000683029.1:n.374A=
ENST00000683211.1:c.1956A=	ENSP00000508257.1:p.Ile652=
ENST00000683250.1:c.*664A=	ENSP00000506847.1:n.*664A=
ENST00000683418.1:n.4303A=
ENST00000684153.1:c.1611A=	ENSP00000506937.1:p.Ile537=
ENST00000684516.1:n.2975A=
ENST00000358487.10:c.1962A= MANE Select	ENSP00000351276.6:p.Ile654=
ENST00000336553.10:c.1689A=	ENSP00000337665.6:p.Ile563=
ENST00000346997.6:c.1956A=	ENSP00000263451.5:p.Ile652=
ENST00000351936.10:c.1962A=	ENSP00000309878.9:p.Ile654=
ENST00000356226.8:c.1611A=	ENSP00000348559.4:p.Ile537=
ENST00000357555.9:c.1695A=	ENSP00000350166.5:p.Ile565=
ENST00000358487.9:c.1962A=	ENSP00000351276.5:p.Ile654=
ENST00000360144.7:c.1698A=	ENSP00000353262.3:p.Ile566=
ENST00000369056.5:c.1965A=	ENSP00000358052.1:p.Ile655=
ENST00000369058.7:c.1965A=	ENSP00000358054.3:p.Ile655=
ENST00000369059.5:c.1620A=	ENSP00000358055.1:p.Ile540=
ENST00000369060.8:c.1614A=	ENSP00000358056.4:p.Ile538=
ENST00000369061.8:c.1626A=	ENSP00000358057.4:p.Ile542=
ENST00000429361.5:c.738A=	ENSP00000404219.1:p.Ile246=
ENST00000457416.6:c.1965A=	ENSP00000410294.2:p.Ile655=
ENST00000478859.5:c.1278A=	ENSP00000474011.1:p.Ile426=
ENST00000604236.5:c.*1009A=	ENSP00000474109.1:n.*1009A=
ENST00000613048.4:c.1695A=	ENSP00000484154.1:p.Ile565=
NM_000141.4:c.1962A=	NP_000132.3:p.Ile654=
NM_001144913.1:c.1965A=	NP_001138385.1:p.Ile655=
NM_001144914.1:c.1626A=	NP_001138386.1:p.Ile542=
NM_001144915.1:c.1695A=	NP_001138387.1:p.Ile565=
NM_001144916.1:c.1617A=	NP_001138388.1:p.Ile539=
NM_001144917.1:c.1614A=	NP_001138389.1:p.Ile538=
NM_001144918.1:c.1611A=	NP_001138390.1:p.Ile537=
NM_001144919.1:c.1698A=	NP_001138391.1:p.Ile566=
NM_022970.3:c.1965A=	NP_075259.4:p.Ile655=
NM_023029.2:c.1695A=	NP_075418.1:p.Ile565=
NR_073009.1:n.2412A=
XM_006717708.2:c.2016A=	XP_006717771.1:p.Ile672=
XM_006717709.2:c.2013A=	XP_006717772.1:p.Ile671=
XM_006717710.2:c.2022A=	XP_006717773.1:p.Ile674=
XM_006717711.2:c.1755A=	XP_006717774.1:p.Ile585=
XM_006717712.2:c.1677A=	XP_006717775.1:p.Ile559=
XM_006717713.2:c.2019A=	XP_006717776.1:p.Ile673=
XM_011539510.1:c.1278A=	XP_011537812.1:p.Ile426=
NM_001320654.1:c.1278A=	NP_001307583.1:p.Ile426=
NM_001320658.1:c.1956A=	NP_001307587.1:p.Ile652=
XM_006717708.3:c.2016A=	XP_006717771.1:p.Ile672=
XM_006717710.4:c.2022A=	XP_006717773.1:p.Ile674=
XM_017015920.2:c.2016A=	XP_016871409.1:p.Ile672=
XM_017015921.2:c.2013A=	XP_016871410.1:p.Ile671=
XM_017015924.2:c.1674A=	XP_016871413.1:p.Ile558=
XM_017015925.2:c.1668A=	XP_016871414.1:p.Ile556=
XM_024447887.1:c.1752A=	XP_024303655.1:p.Ile584=
XM_024447888.1:c.1749A=	XP_024303656.1:p.Ile583=
XM_024447889.1:c.1746A=	XP_024303657.1:p.Ile582=
XM_024447890.1:c.1755A=	XP_024303658.1:p.Ile585=
XM_024447891.1:c.1677A=	XP_024303659.1:p.Ile559=
XM_024447892.1:c.792A=	XP_024303660.1:p.Ile264=
NM_000141.5:c.1962A= MANE Select	NP_000132.3:p.Ile654=
NM_001144917.2:c.1614A=	NP_001138389.1:p.Ile538=
NM_001144918.2:c.1611A=	NP_001138390.1:p.Ile537=
NM_001144919.2:c.1698A=	NP_001138391.1:p.Ile566=
NM_001320658.2:c.1956A=	NP_001307587.1:p.Ile652=
NR_073009.2:n.2398A=
NM_001144915.2:c.1695A=	NP_001138387.1:p.Ile565=
NM_001144916.2:c.1617A=	NP_001138388.1:p.Ile539=
NM_001320654.2:c.1278A=	NP_001307583.1:p.Ile426=