Canonical Allele Identifier: CA471647285

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123247562T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121488048T>A , CM000672.2:g.121488048T>A	GRCh38
NC_000010.10:g.123247562T>A , CM000672.1:g.123247562T>A	GRCh37
NC_000010.9:g.123237552T>A	NCBI36
NG_012449.1:g.115411A>T
NG_012449.2:g.115411A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1932A>T MANE Plus Clinical	ENSP00000410294.2:p.Ala644=
ENST00000351936.11:c.1923A>T	ENSP00000309878.10:p.Ala641=
ENST00000638709.2:c.753A>T	ENSP00000491912.2:p.Ala251=
ENST00000682296.1:n.1271A>T
ENST00000682550.1:c.1578A>T	ENSP00000507633.1:p.Ala526=
ENST00000682772.1:c.753A>T	ENSP00000506848.1:p.Ala251=
ENST00000682904.1:n.749A>T
ENST00000683029.1:n.341A>T
ENST00000683211.1:c.1923A>T	ENSP00000508257.1:p.Ala641=
ENST00000683250.1:c.*631A>T	ENSP00000506847.1:n.*631A>T
ENST00000683418.1:n.4270A>T
ENST00000684153.1:c.1578A>T	ENSP00000506937.1:p.Ala526=
ENST00000684516.1:n.2942A>T
ENST00000358487.10:c.1929A>T MANE Select	ENSP00000351276.6:p.Ala643=
ENST00000336553.10:c.1656A>T	ENSP00000337665.6:p.Ala552=
ENST00000346997.6:c.1923A>T	ENSP00000263451.5:p.Ala641=
ENST00000351936.10:c.1929A>T	ENSP00000309878.9:p.Ala643=
ENST00000356226.8:c.1578A>T	ENSP00000348559.4:p.Ala526=
ENST00000357555.9:c.1662A>T	ENSP00000350166.5:p.Ala554=
ENST00000358487.9:c.1929A>T	ENSP00000351276.5:p.Ala643=
ENST00000360144.7:c.1665A>T	ENSP00000353262.3:p.Ala555=
ENST00000369056.5:c.1932A>T	ENSP00000358052.1:p.Ala644=
ENST00000369058.7:c.1932A>T	ENSP00000358054.3:p.Ala644=
ENST00000369059.5:c.1587A>T	ENSP00000358055.1:p.Ala529=
ENST00000369060.8:c.1581A>T	ENSP00000358056.4:p.Ala527=
ENST00000369061.8:c.1593A>T	ENSP00000358057.4:p.Ala531=
ENST00000429361.5:c.705A>T	ENSP00000404219.1:p.Ala235=
ENST00000457416.6:c.1932A>T	ENSP00000410294.2:p.Ala644=
ENST00000478859.5:c.1245A>T	ENSP00000474011.1:p.Ala415=
ENST00000604236.5:c.*976A>T	ENSP00000474109.1:n.*976A>T
ENST00000613048.4:c.1662A>T	ENSP00000484154.1:p.Ala554=
NM_000141.4:c.1929A>T	NP_000132.3:p.Ala643=
NM_001144913.1:c.1932A>T	NP_001138385.1:p.Ala644=
NM_001144914.1:c.1593A>T	NP_001138386.1:p.Ala531=
NM_001144915.1:c.1662A>T	NP_001138387.1:p.Ala554=
NM_001144916.1:c.1584A>T	NP_001138388.1:p.Ala528=
NM_001144917.1:c.1581A>T	NP_001138389.1:p.Ala527=
NM_001144918.1:c.1578A>T	NP_001138390.1:p.Ala526=
NM_001144919.1:c.1665A>T	NP_001138391.1:p.Ala555=
NM_022970.3:c.1932A>T	NP_075259.4:p.Ala644=
NM_023029.2:c.1662A>T	NP_075418.1:p.Ala554=
NR_073009.1:n.2379A>T
XM_006717708.2:c.1983A>T	XP_006717771.1:p.Ala661=
XM_006717709.2:c.1980A>T	XP_006717772.1:p.Ala660=
XM_006717710.2:c.1989A>T	XP_006717773.1:p.Ala663=
XM_006717711.2:c.1722A>T	XP_006717774.1:p.Ala574=
XM_006717712.2:c.1644A>T	XP_006717775.1:p.Ala548=
XM_006717713.2:c.1986A>T	XP_006717776.1:p.Ala662=
XM_011539510.1:c.1245A>T	XP_011537812.1:p.Ala415=
NM_001320654.1:c.1245A>T	NP_001307583.1:p.Ala415=
NM_001320658.1:c.1923A>T	NP_001307587.1:p.Ala641=
XM_006717708.3:c.1983A>T	XP_006717771.1:p.Ala661=
XM_006717710.4:c.1989A>T	XP_006717773.1:p.Ala663=
XM_017015920.2:c.1983A>T	XP_016871409.1:p.Ala661=
XM_017015921.2:c.1980A>T	XP_016871410.1:p.Ala660=
XM_017015924.2:c.1641A>T	XP_016871413.1:p.Ala547=
XM_017015925.2:c.1635A>T	XP_016871414.1:p.Ala545=
XM_024447887.1:c.1719A>T	XP_024303655.1:p.Ala573=
XM_024447888.1:c.1716A>T	XP_024303656.1:p.Ala572=
XM_024447889.1:c.1713A>T	XP_024303657.1:p.Ala571=
XM_024447890.1:c.1722A>T	XP_024303658.1:p.Ala574=
XM_024447891.1:c.1644A>T	XP_024303659.1:p.Ala548=
XM_024447892.1:c.759A>T	XP_024303660.1:p.Ala253=
NM_000141.5:c.1929A>T MANE Select	NP_000132.3:p.Ala643=
NM_001144917.2:c.1581A>T	NP_001138389.1:p.Ala527=
NM_001144918.2:c.1578A>T	NP_001138390.1:p.Ala526=
NM_001144919.2:c.1665A>T	NP_001138391.1:p.Ala555=
NM_001320658.2:c.1923A>T	NP_001307587.1:p.Ala641=
NR_073009.2:n.2365A>T
NM_001144915.2:c.1662A>T	NP_001138387.1:p.Ala554=
NM_001144916.2:c.1584A>T	NP_001138388.1:p.Ala528=
NM_001320654.2:c.1245A>T	NP_001307583.1:p.Ala415=