Canonical Allele Identifier: CA378323223

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121500910C>A , CM000672.2:g.121500910C>A	GRCh38
NC_000010.10:g.123260424C>A , CM000672.1:g.123260424C>A	GRCh37
NC_000010.9:g.123250414C>A	NCBI36
NG_012449.1:g.102549G>T
NG_012449.2:g.102549G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000141.5:c.1477G>T MANE Select	NP_000132.3:p.Gly493Trp
ENST00000358487.10:c.1477G>T MANE Select	ENSP00000351276.6:p.Gly493Trp
ENST00000457416.7:c.1480G>T MANE Plus Clinical	ENSP00000410294.2:p.Gly494Trp
NM_000141.4:c.1477G>T	NP_000132.3:p.Gly493Trp
NM_001144913.1:c.1480G>T	NP_001138385.1:p.Gly494Trp
NM_001144914.1:c.1141G>T	NP_001138386.1:p.Gly381Trp
NM_001144915.1:c.1210G>T	NP_001138387.1:p.Gly404Trp
NM_001144915.2:c.1210G>T	NP_001138387.1:p.Gly404Trp
NM_001144916.1:c.1132G>T	NP_001138388.1:p.Gly378Trp
NM_001144916.2:c.1132G>T	NP_001138388.1:p.Gly378Trp
NM_001144917.1:c.1129G>T	NP_001138389.1:p.Gly377Trp
NM_001144917.2:c.1129G>T	NP_001138389.1:p.Gly377Trp
NM_001144918.1:c.1126G>T	NP_001138390.1:p.Gly376Trp
NM_001144918.2:c.1126G>T	NP_001138390.1:p.Gly376Trp
NM_001144919.1:c.1213G>T	NP_001138391.1:p.Gly405Trp
NM_001144919.2:c.1213G>T	NP_001138391.1:p.Gly405Trp
NM_001320654.1:c.793G>T	NP_001307583.1:p.Gly265Trp
NM_001320654.2:c.793G>T	NP_001307583.1:p.Gly265Trp
NM_001320658.1:c.1471G>T	NP_001307587.1:p.Gly491Trp
NM_001320658.2:c.1471G>T	NP_001307587.1:p.Gly491Trp
NM_022970.3:c.1480G>T	NP_075259.4:p.Gly494Trp
NM_023029.2:c.1210G>T	NP_075418.1:p.Gly404Trp
NR_073009.1:n.1927G>T
NR_073009.2:n.1913G>T
ENST00000336553.10:c.1204G>T	ENSP00000337665.6:p.Gly402Trp
ENST00000346997.6:c.1471G>T	ENSP00000263451.5:p.Gly491Trp
ENST00000351936.10:c.1477G>T	ENSP00000309878.9:p.Gly493Trp
ENST00000351936.11:c.1471G>T	ENSP00000309878.10:p.Gly491Trp
ENST00000356226.8:c.1126G>T	ENSP00000348559.4:p.Gly376Trp
ENST00000357555.9:c.1210G>T	ENSP00000350166.5:p.Gly404Trp
ENST00000358487.9:c.1477G>T	ENSP00000351276.5:p.Gly493Trp
ENST00000360144.7:c.1213G>T	ENSP00000353262.3:p.Gly405Trp
ENST00000369056.5:c.1480G>T	ENSP00000358052.1:p.Gly494Trp
ENST00000369058.7:c.1480G>T	ENSP00000358054.3:p.Gly494Trp
ENST00000369059.5:c.1135G>T	ENSP00000358055.1:p.Gly379Trp
ENST00000369060.8:c.1129G>T	ENSP00000358056.4:p.Gly377Trp
ENST00000369061.8:c.1141G>T	ENSP00000358057.4:p.Gly381Trp
ENST00000429361.5:c.253G>T	ENSP00000404219.1:p.Gly85Trp
ENST00000457416.6:c.1480G>T	ENSP00000410294.2:p.Gly494Trp
ENST00000478859.5:c.793G>T	ENSP00000474011.1:p.Gly265Trp
ENST00000604236.5:c.*524G>T	ENSP00000474109.1:n.*524G>T
ENST00000613048.4:c.1210G>T	ENSP00000484154.1:p.Gly404Trp
ENST00000638709.2:c.301G>T	ENSP00000491912.2:p.Gly101Trp
ENST00000682296.1:n.819G>T
ENST00000682550.1:c.1126G>T	ENSP00000507633.1:p.Gly376Trp
ENST00000682772.1:c.301G>T	ENSP00000506848.1:p.Gly101Trp
ENST00000682904.1:n.297G>T
ENST00000683211.1:c.1471G>T	ENSP00000508257.1:p.Gly491Trp
ENST00000683250.1:c.*179G>T	ENSP00000506847.1:n.*179G>T
ENST00000683418.1:n.3818G>T
ENST00000684153.1:c.1126G>T	ENSP00000506937.1:p.Gly376Trp
ENST00000684516.1:n.2490G>T
XM_006717708.2:c.1531G>T	XP_006717771.1:p.Gly511Trp
XM_006717708.3:c.1531G>T	XP_006717771.1:p.Gly511Trp
XM_006717709.2:c.1528G>T	XP_006717772.1:p.Gly510Trp
XM_006717710.2:c.1537G>T	XP_006717773.1:p.Gly513Trp
XM_006717710.4:c.1537G>T	XP_006717773.1:p.Gly513Trp
XM_006717711.2:c.1270G>T	XP_006717774.1:p.Gly424Trp
XM_006717712.2:c.1192G>T	XP_006717775.1:p.Gly398Trp
XM_006717713.2:c.1534G>T	XP_006717776.1:p.Gly512Trp
XM_011539510.1:c.793G>T	XP_011537812.1:p.Gly265Trp
XM_017015920.2:c.1531G>T	XP_016871409.1:p.Gly511Trp
XM_017015921.2:c.1528G>T	XP_016871410.1:p.Gly510Trp
XM_017015924.2:c.1189G>T	XP_016871413.1:p.Gly397Trp
XM_017015925.2:c.1183G>T	XP_016871414.1:p.Gly395Trp
XM_024447887.1:c.1267G>T	XP_024303655.1:p.Gly423Trp
XM_024447888.1:c.1264G>T	XP_024303656.1:p.Gly422Trp
XM_024447889.1:c.1261G>T	XP_024303657.1:p.Gly421Trp
XM_024447890.1:c.1270G>T	XP_024303658.1:p.Gly424Trp
XM_024447891.1:c.1192G>T	XP_024303659.1:p.Gly398Trp
XM_024447892.1:c.307G>T	XP_024303660.1:p.Gly103Trp