Canonical Allele Identifier: CA378327130

Gene: FGFR2

Linked Data

• MyVariant Identifiers: chr10:g.123274720T>C (hg19) ; chr10:g.121515206T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121515206T>C , CM000672.2:g.121515206T>C	GRCh38
NC_000010.10:g.123274720T>C , CM000672.1:g.123274720T>C	GRCh37
NC_000010.9:g.123264710T>C	NCBI36
NG_012449.1:g.88253A>G
NG_012449.2:g.88253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1201A>G MANE Plus Clinical	ENSP00000410294.2:p.Met401Val
ENST00000351936.11:c.1198A>G	ENSP00000309878.10:p.Met400Val
ENST00000638709.2:c.28A>G	ENSP00000491912.2:p.Met10Val
ENST00000682296.1:n.546A>G
ENST00000682550.1:c.853A>G	ENSP00000507633.1:p.Met285Val
ENST00000682772.1:c.28A>G	ENSP00000506848.1:p.Met10Val
ENST00000683211.1:c.1198A>G	ENSP00000508257.1:p.Met400Val
ENST00000683250.1:c.404-11265A>G	ENSP00000506847.1:n.404-11265A>G
ENST00000683418.1:n.3545A>G
ENST00000684153.1:c.853A>G	ENSP00000506937.1:p.Met285Val
ENST00000358487.10:c.1198A>G MANE Select	ENSP00000351276.6:p.Met400Val
ENST00000336553.10:c.931A>G	ENSP00000337665.6:p.Met311Val
ENST00000346997.6:c.1198A>G	ENSP00000263451.5:p.Met400Val
ENST00000351936.10:c.1204A>G	ENSP00000309878.9:p.Met402Val
ENST00000356226.8:c.853A>G	ENSP00000348559.4:p.Met285Val
ENST00000357555.9:c.931A>G	ENSP00000350166.5:p.Met311Val
ENST00000358487.9:c.1198A>G	ENSP00000351276.5:p.Met400Val
ENST00000360144.7:c.934A>G	ENSP00000353262.3:p.Met312Val
ENST00000369056.5:c.1201A>G	ENSP00000358052.1:p.Met401Val
ENST00000369058.7:c.1201A>G	ENSP00000358054.3:p.Met401Val
ENST00000369059.5:c.856A>G	ENSP00000358055.1:p.Met286Val
ENST00000369060.8:c.939+4773A>G	ENSP00000358056.4:n.939+4773A>G
ENST00000369061.8:c.862A>G	ENSP00000358057.4:p.Met288Val
ENST00000457416.6:c.1201A>G	ENSP00000410294.2:p.Met401Val
ENST00000478859.5:c.514A>G	ENSP00000474011.1:p.Met172Val
ENST00000604236.5:c.*245A>G	ENSP00000474109.1:n.*245A>G
ENST00000613048.4:c.931A>G	ENSP00000484154.1:p.Met311Val
NM_000141.4:c.1198A>G	NP_000132.3:p.Met400Val
NM_001144913.1:c.1201A>G	NP_001138385.1:p.Met401Val
NM_001144914.1:c.862A>G	NP_001138386.1:p.Met288Val
NM_001144915.1:c.931A>G	NP_001138387.1:p.Met311Val
NM_001144916.1:c.853A>G	NP_001138388.1:p.Met285Val
NM_001144917.1:c.939+4773A>G	NP_001138389.1:n.939+4773A>G
NM_001144918.1:c.853A>G	NP_001138390.1:p.Met285Val
NM_001144919.1:c.934A>G	NP_001138391.1:p.Met312Val
NM_022970.3:c.1201A>G	NP_075259.4:p.Met401Val
NM_023029.2:c.931A>G	NP_075418.1:p.Met311Val
NR_073009.1:n.1648A>G
XM_006717708.2:c.1258A>G	XP_006717771.1:p.Met420Val
XM_006717709.2:c.1255A>G	XP_006717772.1:p.Met419Val
XM_006717710.2:c.1258A>G	XP_006717773.1:p.Met420Val
XM_006717711.2:c.991A>G	XP_006717774.1:p.Met331Val
XM_006717712.2:c.913A>G	XP_006717775.1:p.Met305Val
XM_006717713.2:c.1255A>G	XP_006717776.1:p.Met419Val
XM_011539510.1:c.514A>G	XP_011537812.1:p.Met172Val
NM_001320654.1:c.514A>G	NP_001307583.1:p.Met172Val
NM_001320658.1:c.1198A>G	NP_001307587.1:p.Met400Val
XM_006717708.3:c.1258A>G	XP_006717771.1:p.Met420Val
XM_006717710.4:c.1258A>G	XP_006717773.1:p.Met420Val
XM_017015920.2:c.1258A>G	XP_016871409.1:p.Met420Val
XM_017015921.2:c.1255A>G	XP_016871410.1:p.Met419Val
XM_017015924.2:c.910A>G	XP_016871413.1:p.Met304Val
XM_017015925.2:c.910A>G	XP_016871414.1:p.Met304Val
XM_024447887.1:c.988A>G	XP_024303655.1:p.Met330Val
XM_024447888.1:c.991A>G	XP_024303656.1:p.Met331Val
XM_024447889.1:c.988A>G	XP_024303657.1:p.Met330Val
XM_024447890.1:c.991A>G	XP_024303658.1:p.Met331Val
XM_024447891.1:c.913A>G	XP_024303659.1:p.Met305Val
XM_024447892.1:c.28A>G	XP_024303660.1:p.Met10Val
NM_000141.5:c.1198A>G MANE Select	NP_000132.3:p.Met400Val
NM_001144917.2:c.939+4773A>G	NP_001138389.1:n.939+4773A>G
NM_001144918.2:c.853A>G	NP_001138390.1:p.Met285Val
NM_001144919.2:c.934A>G	NP_001138391.1:p.Met312Val
NM_001320658.2:c.1198A>G	NP_001307587.1:p.Met400Val
NR_073009.2:n.1634A>G
NM_001144915.2:c.931A>G	NP_001138387.1:p.Met311Val
NM_001144916.2:c.853A>G	NP_001138388.1:p.Met285Val
NM_001320654.2:c.514A>G	NP_001307583.1:p.Met172Val