Canonical Allele Identifier: CA5720766

Gene: FGFR2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.121503880C>T , CM000672.2:g.121503880C>T	GRCh38
NC_000010.10:g.123263394C>T , CM000672.1:g.123263394C>T	GRCh37
NC_000010.9:g.123253384C>T	NCBI36
NG_012449.1:g.99579G>A
NG_012449.2:g.99579G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457416.7:c.1352G>A MANE Plus Clinical	ENSP00000410294.2:p.Arg451His
ENST00000351936.11:c.1343G>A	ENSP00000309878.10:p.Arg448His
ENST00000638709.2:c.173G>A	ENSP00000491912.2:p.Arg58His
ENST00000682296.1:n.691G>A
ENST00000682550.1:c.998G>A	ENSP00000507633.1:p.Arg333His
ENST00000682772.1:c.173G>A	ENSP00000506848.1:p.Arg58His
ENST00000682904.1:n.169G>A
ENST00000683211.1:c.1343G>A	ENSP00000508257.1:p.Arg448His
ENST00000683250.1:c.*51G>A	ENSP00000506847.1:n.*51G>A
ENST00000683418.1:n.3690G>A
ENST00000684153.1:c.998G>A	ENSP00000506937.1:p.Arg333His
ENST00000684516.1:n.2362G>A
ENST00000358487.10:c.1349G>A MANE Select	ENSP00000351276.6:p.Arg450His
ENST00000336553.10:c.1076G>A	ENSP00000337665.6:p.Arg359His
ENST00000346997.6:c.1343G>A	ENSP00000263451.5:p.Arg448His
ENST00000351936.10:c.1349G>A	ENSP00000309878.9:p.Arg450His
ENST00000356226.8:c.998G>A	ENSP00000348559.4:p.Arg333His
ENST00000357555.9:c.1082G>A	ENSP00000350166.5:p.Arg361His
ENST00000358487.9:c.1349G>A	ENSP00000351276.5:p.Arg450His
ENST00000360144.7:c.1085G>A	ENSP00000353262.3:p.Arg362His
ENST00000369056.5:c.1352G>A	ENSP00000358052.1:p.Arg451His
ENST00000369058.7:c.1352G>A	ENSP00000358054.3:p.Arg451His
ENST00000369059.5:c.1007G>A	ENSP00000358055.1:p.Arg336His
ENST00000369060.8:c.1001G>A	ENSP00000358056.4:p.Arg334His
ENST00000369061.8:c.1013G>A	ENSP00000358057.4:p.Arg338His
ENST00000429361.5:c.125G>A	ENSP00000404219.1:p.Arg42His
ENST00000457416.6:c.1352G>A	ENSP00000410294.2:p.Arg451His
ENST00000478859.5:c.665G>A	ENSP00000474011.1:p.Arg222His
ENST00000604236.5:c.*396G>A	ENSP00000474109.1:n.*396G>A
ENST00000613048.4:c.1082G>A	ENSP00000484154.1:p.Arg361His
NM_000141.4:c.1349G>A	NP_000132.3:p.Arg450His
NM_001144913.1:c.1352G>A	NP_001138385.1:p.Arg451His
NM_001144914.1:c.1013G>A	NP_001138386.1:p.Arg338His
NM_001144915.1:c.1082G>A	NP_001138387.1:p.Arg361His
NM_001144916.1:c.1004G>A	NP_001138388.1:p.Arg335His
NM_001144917.1:c.1001G>A	NP_001138389.1:p.Arg334His
NM_001144918.1:c.998G>A	NP_001138390.1:p.Arg333His
NM_001144919.1:c.1085G>A	NP_001138391.1:p.Arg362His
NM_022970.3:c.1352G>A	NP_075259.4:p.Arg451His
NM_023029.2:c.1082G>A	NP_075418.1:p.Arg361His
NR_073009.1:n.1799G>A
XM_006717708.2:c.1403G>A	XP_006717771.1:p.Arg468His
XM_006717709.2:c.1400G>A	XP_006717772.1:p.Arg467His
XM_006717710.2:c.1409G>A	XP_006717773.1:p.Arg470His
XM_006717711.2:c.1142G>A	XP_006717774.1:p.Arg381His
XM_006717712.2:c.1064G>A	XP_006717775.1:p.Arg355His
XM_006717713.2:c.1406G>A	XP_006717776.1:p.Arg469His
XM_011539510.1:c.665G>A	XP_011537812.1:p.Arg222His
NM_001320654.1:c.665G>A	NP_001307583.1:p.Arg222His
NM_001320658.1:c.1343G>A	NP_001307587.1:p.Arg448His
XM_006717708.3:c.1403G>A	XP_006717771.1:p.Arg468His
XM_006717710.4:c.1409G>A	XP_006717773.1:p.Arg470His
XM_017015920.2:c.1403G>A	XP_016871409.1:p.Arg468His
XM_017015921.2:c.1400G>A	XP_016871410.1:p.Arg467His
XM_017015924.2:c.1061G>A	XP_016871413.1:p.Arg354His
XM_017015925.2:c.1055G>A	XP_016871414.1:p.Arg352His
XM_024447887.1:c.1139G>A	XP_024303655.1:p.Arg380His
XM_024447888.1:c.1136G>A	XP_024303656.1:p.Arg379His
XM_024447889.1:c.1133G>A	XP_024303657.1:p.Arg378His
XM_024447890.1:c.1142G>A	XP_024303658.1:p.Arg381His
XM_024447891.1:c.1064G>A	XP_024303659.1:p.Arg355His
XM_024447892.1:c.179G>A	XP_024303660.1:p.Arg60His
NM_000141.5:c.1349G>A MANE Select	NP_000132.3:p.Arg450His
NM_001144917.2:c.1001G>A	NP_001138389.1:p.Arg334His
NM_001144918.2:c.998G>A	NP_001138390.1:p.Arg333His
NM_001144919.2:c.1085G>A	NP_001138391.1:p.Arg362His
NM_001320658.2:c.1343G>A	NP_001307587.1:p.Arg448His
NR_073009.2:n.1785G>A
NM_001144915.2:c.1082G>A	NP_001138387.1:p.Arg361His
NM_001144916.2:c.1004G>A	NP_001138388.1:p.Arg335His
NM_001320654.2:c.665G>A	NP_001307583.1:p.Arg222His