Canonical Allele Identifier: CA378321387

Gene: FGFR2

Linked Data

• dbSNP Id: rs2133972282
• MyVariant Identifiers: chr10:g.123258027C>G (hg19) ; chr10:g.121498513C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121498513C>G , CM000672.2:g.121498513C>G	GRCh38
NC_000010.10:g.123258027C>G , CM000672.1:g.123258027C>G	GRCh37
NC_000010.9:g.123248017C>G	NCBI36
NG_012449.1:g.104946G>C
NG_012449.2:g.104946G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1657G>C MANE Plus Clinical	ENSP00000410294.2:p.Gly553Arg
ENST00000351936.11:c.1648G>C	ENSP00000309878.10:p.Gly550Arg
ENST00000638709.2:c.478G>C	ENSP00000491912.2:p.Gly160Arg
ENST00000682296.1:n.996G>C
ENST00000682550.1:c.1303G>C	ENSP00000507633.1:p.Gly435Arg
ENST00000682772.1:c.478G>C	ENSP00000506848.1:p.Gly160Arg
ENST00000682904.1:n.474G>C
ENST00000683211.1:c.1648G>C	ENSP00000508257.1:p.Gly550Arg
ENST00000683250.1:c.*356G>C	ENSP00000506847.1:n.*356G>C
ENST00000683418.1:n.3995G>C
ENST00000684153.1:c.1303G>C	ENSP00000506937.1:p.Gly435Arg
ENST00000684516.1:n.2667G>C
ENST00000358487.10:c.1654G>C MANE Select	ENSP00000351276.6:p.Gly552Arg
ENST00000336553.10:c.1381G>C	ENSP00000337665.6:p.Gly461Arg
ENST00000346997.6:c.1648G>C	ENSP00000263451.5:p.Gly550Arg
ENST00000351936.10:c.1654G>C	ENSP00000309878.9:p.Gly552Arg
ENST00000356226.8:c.1303G>C	ENSP00000348559.4:p.Gly435Arg
ENST00000357555.9:c.1387G>C	ENSP00000350166.5:p.Gly463Arg
ENST00000358487.9:c.1654G>C	ENSP00000351276.5:p.Gly552Arg
ENST00000360144.7:c.1390G>C	ENSP00000353262.3:p.Gly464Arg
ENST00000369056.5:c.1657G>C	ENSP00000358052.1:p.Gly553Arg
ENST00000369058.7:c.1657G>C	ENSP00000358054.3:p.Gly553Arg
ENST00000369059.5:c.1312G>C	ENSP00000358055.1:p.Gly438Arg
ENST00000369060.8:c.1306G>C	ENSP00000358056.4:p.Gly436Arg
ENST00000369061.8:c.1318G>C	ENSP00000358057.4:p.Gly440Arg
ENST00000429361.5:c.430G>C	ENSP00000404219.1:p.Gly144Arg
ENST00000457416.6:c.1657G>C	ENSP00000410294.2:p.Gly553Arg
ENST00000478859.5:c.970G>C	ENSP00000474011.1:p.Gly324Arg
ENST00000604236.5:c.*701G>C	ENSP00000474109.1:n.*701G>C
ENST00000613048.4:c.1387G>C	ENSP00000484154.1:p.Gly463Arg
NM_000141.4:c.1654G>C	NP_000132.3:p.Gly552Arg
NM_001144913.1:c.1657G>C	NP_001138385.1:p.Gly553Arg
NM_001144914.1:c.1318G>C	NP_001138386.1:p.Gly440Arg
NM_001144915.1:c.1387G>C	NP_001138387.1:p.Gly463Arg
NM_001144916.1:c.1309G>C	NP_001138388.1:p.Gly437Arg
NM_001144917.1:c.1306G>C	NP_001138389.1:p.Gly436Arg
NM_001144918.1:c.1303G>C	NP_001138390.1:p.Gly435Arg
NM_001144919.1:c.1390G>C	NP_001138391.1:p.Gly464Arg
NM_022970.3:c.1657G>C	NP_075259.4:p.Gly553Arg
NM_023029.2:c.1387G>C	NP_075418.1:p.Gly463Arg
NR_073009.1:n.2104G>C
XM_006717708.2:c.1708G>C	XP_006717771.1:p.Gly570Arg
XM_006717709.2:c.1705G>C	XP_006717772.1:p.Gly569Arg
XM_006717710.2:c.1714G>C	XP_006717773.1:p.Gly572Arg
XM_006717711.2:c.1447G>C	XP_006717774.1:p.Gly483Arg
XM_006717712.2:c.1369G>C	XP_006717775.1:p.Gly457Arg
XM_006717713.2:c.1711G>C	XP_006717776.1:p.Gly571Arg
XM_011539510.1:c.970G>C	XP_011537812.1:p.Gly324Arg
NM_001320654.1:c.970G>C	NP_001307583.1:p.Gly324Arg
NM_001320658.1:c.1648G>C	NP_001307587.1:p.Gly550Arg
XM_006717708.3:c.1708G>C	XP_006717771.1:p.Gly570Arg
XM_006717710.4:c.1714G>C	XP_006717773.1:p.Gly572Arg
XM_017015920.2:c.1708G>C	XP_016871409.1:p.Gly570Arg
XM_017015921.2:c.1705G>C	XP_016871410.1:p.Gly569Arg
XM_017015924.2:c.1366G>C	XP_016871413.1:p.Gly456Arg
XM_017015925.2:c.1360G>C	XP_016871414.1:p.Gly454Arg
XM_024447887.1:c.1444G>C	XP_024303655.1:p.Gly482Arg
XM_024447888.1:c.1441G>C	XP_024303656.1:p.Gly481Arg
XM_024447889.1:c.1438G>C	XP_024303657.1:p.Gly480Arg
XM_024447890.1:c.1447G>C	XP_024303658.1:p.Gly483Arg
XM_024447891.1:c.1369G>C	XP_024303659.1:p.Gly457Arg
XM_024447892.1:c.484G>C	XP_024303660.1:p.Gly162Arg
NM_000141.5:c.1654G>C MANE Select	NP_000132.3:p.Gly552Arg
NM_001144917.2:c.1306G>C	NP_001138389.1:p.Gly436Arg
NM_001144918.2:c.1303G>C	NP_001138390.1:p.Gly435Arg
NM_001144919.2:c.1390G>C	NP_001138391.1:p.Gly464Arg
NM_001320658.2:c.1648G>C	NP_001307587.1:p.Gly550Arg
NR_073009.2:n.2090G>C
NM_001144915.2:c.1387G>C	NP_001138387.1:p.Gly463Arg
NM_001144916.2:c.1309G>C	NP_001138388.1:p.Gly437Arg
NM_001320654.2:c.970G>C	NP_001307583.1:p.Gly324Arg