Canonical Allele Identifier: CA378327372

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123274806G>T (hg19) ; chr10:g.121515292G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515292G>T , CM000672.2:g.121515292G>T	GRCh38
NC_000010.10:g.123274806G>T , CM000672.1:g.123274806G>T	GRCh37
NC_000010.9:g.123264796G>T	NCBI36
NG_012449.1:g.88167C>A
NG_012449.2:g.88167C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1115C>A MANE Plus Clinical	ENSP00000410294.2:p.Ala372Asp
ENST00000351936.11:c.1112C>A	ENSP00000309878.10:p.Ala371Asp
ENST00000638709.2:c.-59C>A	ENSP00000491912.2:n.-59C>A
ENST00000682296.1:n.460C>A
ENST00000682550.1:c.767C>A	ENSP00000507633.1:p.Ala256Asp
ENST00000682772.1:c.-59C>A	ENSP00000506848.1:n.-59C>A
ENST00000683211.1:c.1112C>A	ENSP00000508257.1:p.Ala371Asp
ENST00000683250.1:c.404-11351C>A	ENSP00000506847.1:n.404-11351C>A
ENST00000683418.1:n.3459C>A
ENST00000684153.1:c.767C>A	ENSP00000506937.1:p.Ala256Asp
ENST00000358487.10:c.1112C>A MANE Select	ENSP00000351276.6:p.Ala371Asp
ENST00000336553.10:c.845C>A	ENSP00000337665.6:p.Ala282Asp
ENST00000346997.6:c.1112C>A	ENSP00000263451.5:p.Ala371Asp
ENST00000351936.10:c.1118C>A	ENSP00000309878.9:p.Ala373Asp
ENST00000356226.8:c.767C>A	ENSP00000348559.4:p.Ala256Asp
ENST00000357555.9:c.845C>A	ENSP00000350166.5:p.Ala282Asp
ENST00000358487.9:c.1112C>A	ENSP00000351276.5:p.Ala371Asp
ENST00000360144.7:c.848C>A	ENSP00000353262.3:p.Ala283Asp
ENST00000369056.5:c.1115C>A	ENSP00000358052.1:p.Ala372Asp
ENST00000369058.7:c.1115C>A	ENSP00000358054.3:p.Ala372Asp
ENST00000369059.5:c.770C>A	ENSP00000358055.1:p.Ala257Asp
ENST00000369060.8:c.939+4687C>A	ENSP00000358056.4:n.939+4687C>A
ENST00000369061.8:c.776C>A	ENSP00000358057.4:p.Ala259Asp
ENST00000457416.6:c.1115C>A	ENSP00000410294.2:p.Ala372Asp
ENST00000463870.5:n.321C>A
ENST00000478859.5:c.428C>A	ENSP00000474011.1:p.Ala143Asp
ENST00000604236.5:c.*159C>A	ENSP00000474109.1:n.*159C>A
ENST00000613048.4:c.845C>A	ENSP00000484154.1:p.Ala282Asp
NM_000141.4:c.1112C>A	NP_000132.3:p.Ala371Asp
NM_001144913.1:c.1115C>A	NP_001138385.1:p.Ala372Asp
NM_001144914.1:c.776C>A	NP_001138386.1:p.Ala259Asp
NM_001144915.1:c.845C>A	NP_001138387.1:p.Ala282Asp
NM_001144916.1:c.767C>A	NP_001138388.1:p.Ala256Asp
NM_001144917.1:c.939+4687C>A	NP_001138389.1:n.939+4687C>A
NM_001144918.1:c.767C>A	NP_001138390.1:p.Ala256Asp
NM_001144919.1:c.848C>A	NP_001138391.1:p.Ala283Asp
NM_022970.3:c.1115C>A	NP_075259.4:p.Ala372Asp
NM_023029.2:c.845C>A	NP_075418.1:p.Ala282Asp
NR_073009.1:n.1562C>A
XM_006717708.2:c.1172C>A	XP_006717771.1:p.Ala391Asp
XM_006717709.2:c.1169C>A	XP_006717772.1:p.Ala390Asp
XM_006717710.2:c.1172C>A	XP_006717773.1:p.Ala391Asp
XM_006717711.2:c.905C>A	XP_006717774.1:p.Ala302Asp
XM_006717712.2:c.827C>A	XP_006717775.1:p.Ala276Asp
XM_006717713.2:c.1169C>A	XP_006717776.1:p.Ala390Asp
XM_011539510.1:c.428C>A	XP_011537812.1:p.Ala143Asp
NM_001320654.1:c.428C>A	NP_001307583.1:p.Ala143Asp
NM_001320658.1:c.1112C>A	NP_001307587.1:p.Ala371Asp
XM_006717708.3:c.1172C>A	XP_006717771.1:p.Ala391Asp
XM_006717710.4:c.1172C>A	XP_006717773.1:p.Ala391Asp
XM_017015920.2:c.1172C>A	XP_016871409.1:p.Ala391Asp
XM_017015921.2:c.1169C>A	XP_016871410.1:p.Ala390Asp
XM_017015924.2:c.824C>A	XP_016871413.1:p.Ala275Asp
XM_017015925.2:c.824C>A	XP_016871414.1:p.Ala275Asp
XM_024447887.1:c.902C>A	XP_024303655.1:p.Ala301Asp
XM_024447888.1:c.905C>A	XP_024303656.1:p.Ala302Asp
XM_024447889.1:c.902C>A	XP_024303657.1:p.Ala301Asp
XM_024447890.1:c.905C>A	XP_024303658.1:p.Ala302Asp
XM_024447891.1:c.827C>A	XP_024303659.1:p.Ala276Asp
XM_024447892.1:c.-59C>A	XP_024303660.1:n.-59C>A
NM_000141.5:c.1112C>A MANE Select	NP_000132.3:p.Ala371Asp
NM_001144917.2:c.939+4687C>A	NP_001138389.1:n.939+4687C>A
NM_001144918.2:c.767C>A	NP_001138390.1:p.Ala256Asp
NM_001144919.2:c.848C>A	NP_001138391.1:p.Ala283Asp
NM_001320658.2:c.1112C>A	NP_001307587.1:p.Ala371Asp
NR_073009.2:n.1548C>A
NM_001144915.2:c.845C>A	NP_001138387.1:p.Ala282Asp
NM_001144916.2:c.767C>A	NP_001138388.1:p.Ala256Asp
NM_001320654.2:c.428C>A	NP_001307583.1:p.Ala143Asp