Canonical Allele Identifier: CA471649445

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123258082T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121498568T>G , CM000672.2:g.121498568T>G	GRCh38
NC_000010.10:g.123258082T>G , CM000672.1:g.123258082T>G	GRCh37
NC_000010.9:g.123248072T>G	NCBI36
NG_012449.1:g.104891A>C
NG_012449.2:g.104891A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1602A>C MANE Plus Clinical	ENSP00000410294.2:p.Ser534=
ENST00000351936.11:c.1593A>C	ENSP00000309878.10:p.Ser531=
ENST00000638709.2:c.423A>C	ENSP00000491912.2:p.Ser141=
ENST00000682296.1:n.941A>C
ENST00000682550.1:c.1248A>C	ENSP00000507633.1:p.Ser416=
ENST00000682772.1:c.423A>C	ENSP00000506848.1:p.Ser141=
ENST00000682904.1:n.419A>C
ENST00000683211.1:c.1593A>C	ENSP00000508257.1:p.Ser531=
ENST00000683250.1:c.*301A>C	ENSP00000506847.1:n.*301A>C
ENST00000683418.1:n.3940A>C
ENST00000684153.1:c.1248A>C	ENSP00000506937.1:p.Ser416=
ENST00000684516.1:n.2612A>C
ENST00000358487.10:c.1599A>C MANE Select	ENSP00000351276.6:p.Ser533=
ENST00000336553.10:c.1326A>C	ENSP00000337665.6:p.Ser442=
ENST00000346997.6:c.1593A>C	ENSP00000263451.5:p.Ser531=
ENST00000351936.10:c.1599A>C	ENSP00000309878.9:p.Ser533=
ENST00000356226.8:c.1248A>C	ENSP00000348559.4:p.Ser416=
ENST00000357555.9:c.1332A>C	ENSP00000350166.5:p.Ser444=
ENST00000358487.9:c.1599A>C	ENSP00000351276.5:p.Ser533=
ENST00000360144.7:c.1335A>C	ENSP00000353262.3:p.Ser445=
ENST00000369056.5:c.1602A>C	ENSP00000358052.1:p.Ser534=
ENST00000369058.7:c.1602A>C	ENSP00000358054.3:p.Ser534=
ENST00000369059.5:c.1257A>C	ENSP00000358055.1:p.Ser419=
ENST00000369060.8:c.1251A>C	ENSP00000358056.4:p.Ser417=
ENST00000369061.8:c.1263A>C	ENSP00000358057.4:p.Ser421=
ENST00000429361.5:c.375A>C	ENSP00000404219.1:p.Ser125=
ENST00000457416.6:c.1602A>C	ENSP00000410294.2:p.Ser534=
ENST00000478859.5:c.915A>C	ENSP00000474011.1:p.Ser305=
ENST00000604236.5:c.*646A>C	ENSP00000474109.1:n.*646A>C
ENST00000613048.4:c.1332A>C	ENSP00000484154.1:p.Ser444=
NM_000141.4:c.1599A>C	NP_000132.3:p.Ser533=
NM_001144913.1:c.1602A>C	NP_001138385.1:p.Ser534=
NM_001144914.1:c.1263A>C	NP_001138386.1:p.Ser421=
NM_001144915.1:c.1332A>C	NP_001138387.1:p.Ser444=
NM_001144916.1:c.1254A>C	NP_001138388.1:p.Ser418=
NM_001144917.1:c.1251A>C	NP_001138389.1:p.Ser417=
NM_001144918.1:c.1248A>C	NP_001138390.1:p.Ser416=
NM_001144919.1:c.1335A>C	NP_001138391.1:p.Ser445=
NM_022970.3:c.1602A>C	NP_075259.4:p.Ser534=
NM_023029.2:c.1332A>C	NP_075418.1:p.Ser444=
NR_073009.1:n.2049A>C
XM_006717708.2:c.1653A>C	XP_006717771.1:p.Ser551=
XM_006717709.2:c.1650A>C	XP_006717772.1:p.Ser550=
XM_006717710.2:c.1659A>C	XP_006717773.1:p.Ser553=
XM_006717711.2:c.1392A>C	XP_006717774.1:p.Ser464=
XM_006717712.2:c.1314A>C	XP_006717775.1:p.Ser438=
XM_006717713.2:c.1656A>C	XP_006717776.1:p.Ser552=
XM_011539510.1:c.915A>C	XP_011537812.1:p.Ser305=
NM_001320654.1:c.915A>C	NP_001307583.1:p.Ser305=
NM_001320658.1:c.1593A>C	NP_001307587.1:p.Ser531=
XM_006717708.3:c.1653A>C	XP_006717771.1:p.Ser551=
XM_006717710.4:c.1659A>C	XP_006717773.1:p.Ser553=
XM_017015920.2:c.1653A>C	XP_016871409.1:p.Ser551=
XM_017015921.2:c.1650A>C	XP_016871410.1:p.Ser550=
XM_017015924.2:c.1311A>C	XP_016871413.1:p.Ser437=
XM_017015925.2:c.1305A>C	XP_016871414.1:p.Ser435=
XM_024447887.1:c.1389A>C	XP_024303655.1:p.Ser463=
XM_024447888.1:c.1386A>C	XP_024303656.1:p.Ser462=
XM_024447889.1:c.1383A>C	XP_024303657.1:p.Ser461=
XM_024447890.1:c.1392A>C	XP_024303658.1:p.Ser464=
XM_024447891.1:c.1314A>C	XP_024303659.1:p.Ser438=
XM_024447892.1:c.429A>C	XP_024303660.1:p.Ser143=
NM_000141.5:c.1599A>C MANE Select	NP_000132.3:p.Ser533=
NM_001144917.2:c.1251A>C	NP_001138389.1:p.Ser417=
NM_001144918.2:c.1248A>C	NP_001138390.1:p.Ser416=
NM_001144919.2:c.1335A>C	NP_001138391.1:p.Ser445=
NM_001320658.2:c.1593A>C	NP_001307587.1:p.Ser531=
NR_073009.2:n.2035A>C
NM_001144915.2:c.1332A>C	NP_001138387.1:p.Ser444=
NM_001144916.2:c.1254A>C	NP_001138388.1:p.Ser418=
NM_001320654.2:c.915A>C	NP_001307583.1:p.Ser305=