Canonical Allele Identifier: CA378321486

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133973526
• MyVariant Identifiers: chr10:g.123258051G>C (hg19) ; chr10:g.121498537G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121498537G>C , CM000672.2:g.121498537G>C	GRCh38
NC_000010.10:g.123258051G>C , CM000672.1:g.123258051G>C	GRCh37
NC_000010.9:g.123248041G>C	NCBI36
NG_012449.1:g.104922C>G
NG_012449.2:g.104922C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000457416.7:c.1633C>G MANE Plus Clinical	ENSP00000410294.2:p.His545Asp
ENST00000351936.11:c.1624C>G	ENSP00000309878.10:p.His542Asp
ENST00000638709.2:c.454C>G	ENSP00000491912.2:p.His152Asp
ENST00000682296.1:n.972C>G
ENST00000682550.1:c.1279C>G	ENSP00000507633.1:p.His427Asp
ENST00000682772.1:c.454C>G	ENSP00000506848.1:p.His152Asp
ENST00000682904.1:n.450C>G
ENST00000683211.1:c.1624C>G	ENSP00000508257.1:p.His542Asp
ENST00000683250.1:c.*332C>G	ENSP00000506847.1:n.*332C>G
ENST00000683418.1:n.3971C>G
ENST00000684153.1:c.1279C>G	ENSP00000506937.1:p.His427Asp
ENST00000684516.1:n.2643C>G
ENST00000358487.10:c.1630C>G MANE Select	ENSP00000351276.6:p.His544Asp
ENST00000336553.10:c.1357C>G	ENSP00000337665.6:p.His453Asp
ENST00000346997.6:c.1624C>G	ENSP00000263451.5:p.His542Asp
ENST00000351936.10:c.1630C>G	ENSP00000309878.9:p.His544Asp
ENST00000356226.8:c.1279C>G	ENSP00000348559.4:p.His427Asp
ENST00000357555.9:c.1363C>G	ENSP00000350166.5:p.His455Asp
ENST00000358487.9:c.1630C>G	ENSP00000351276.5:p.His544Asp
ENST00000360144.7:c.1366C>G	ENSP00000353262.3:p.His456Asp
ENST00000369056.5:c.1633C>G	ENSP00000358052.1:p.His545Asp
ENST00000369058.7:c.1633C>G	ENSP00000358054.3:p.His545Asp
ENST00000369059.5:c.1288C>G	ENSP00000358055.1:p.His430Asp
ENST00000369060.8:c.1282C>G	ENSP00000358056.4:p.His428Asp
ENST00000369061.8:c.1294C>G	ENSP00000358057.4:p.His432Asp
ENST00000429361.5:c.406C>G	ENSP00000404219.1:p.His136Asp
ENST00000457416.6:c.1633C>G	ENSP00000410294.2:p.His545Asp
ENST00000478859.5:c.946C>G	ENSP00000474011.1:p.His316Asp
ENST00000604236.5:c.*677C>G	ENSP00000474109.1:n.*677C>G
ENST00000613048.4:c.1363C>G	ENSP00000484154.1:p.His455Asp
NM_000141.4:c.1630C>G	NP_000132.3:p.His544Asp
NM_001144913.1:c.1633C>G	NP_001138385.1:p.His545Asp
NM_001144914.1:c.1294C>G	NP_001138386.1:p.His432Asp
NM_001144915.1:c.1363C>G	NP_001138387.1:p.His455Asp
NM_001144916.1:c.1285C>G	NP_001138388.1:p.His429Asp
NM_001144917.1:c.1282C>G	NP_001138389.1:p.His428Asp
NM_001144918.1:c.1279C>G	NP_001138390.1:p.His427Asp
NM_001144919.1:c.1366C>G	NP_001138391.1:p.His456Asp
NM_022970.3:c.1633C>G	NP_075259.4:p.His545Asp
NM_023029.2:c.1363C>G	NP_075418.1:p.His455Asp
NR_073009.1:n.2080C>G
XM_006717708.2:c.1684C>G	XP_006717771.1:p.His562Asp
XM_006717709.2:c.1681C>G	XP_006717772.1:p.His561Asp
XM_006717710.2:c.1690C>G	XP_006717773.1:p.His564Asp
XM_006717711.2:c.1423C>G	XP_006717774.1:p.His475Asp
XM_006717712.2:c.1345C>G	XP_006717775.1:p.His449Asp
XM_006717713.2:c.1687C>G	XP_006717776.1:p.His563Asp
XM_011539510.1:c.946C>G	XP_011537812.1:p.His316Asp
NM_001320654.1:c.946C>G	NP_001307583.1:p.His316Asp
NM_001320658.1:c.1624C>G	NP_001307587.1:p.His542Asp
XM_006717708.3:c.1684C>G	XP_006717771.1:p.His562Asp
XM_006717710.4:c.1690C>G	XP_006717773.1:p.His564Asp
XM_017015920.2:c.1684C>G	XP_016871409.1:p.His562Asp
XM_017015921.2:c.1681C>G	XP_016871410.1:p.His561Asp
XM_017015924.2:c.1342C>G	XP_016871413.1:p.His448Asp
XM_017015925.2:c.1336C>G	XP_016871414.1:p.His446Asp
XM_024447887.1:c.1420C>G	XP_024303655.1:p.His474Asp
XM_024447888.1:c.1417C>G	XP_024303656.1:p.His473Asp
XM_024447889.1:c.1414C>G	XP_024303657.1:p.His472Asp
XM_024447890.1:c.1423C>G	XP_024303658.1:p.His475Asp
XM_024447891.1:c.1345C>G	XP_024303659.1:p.His449Asp
XM_024447892.1:c.460C>G	XP_024303660.1:p.His154Asp
NM_000141.5:c.1630C>G MANE Select	NP_000132.3:p.His544Asp
NM_001144917.2:c.1282C>G	NP_001138389.1:p.His428Asp
NM_001144918.2:c.1279C>G	NP_001138390.1:p.His427Asp
NM_001144919.2:c.1366C>G	NP_001138391.1:p.His456Asp
NM_001320658.2:c.1624C>G	NP_001307587.1:p.His542Asp
NR_073009.2:n.2066C>G
NM_001144915.2:c.1363C>G	NP_001138387.1:p.His455Asp
NM_001144916.2:c.1285C>G	NP_001138388.1:p.His429Asp
NM_001320654.2:c.946C>G	NP_001307583.1:p.His316Asp