Canonical Allele Identifier: CA1941017699
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498519G= , CM000672.2:g.121498519G= GRCh38
NC_000010.10:g.123258033G= , CM000672.1:g.123258033G= GRCh37
NC_000010.9:g.123248023G= NCBI36
NG_012449.1:g.104940C=
NG_012449.2:g.104940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1651C= MANE Plus Clinical ENSP00000410294.2:p.Leu551=
ENST00000351936.11:c.1642C= ENSP00000309878.10:p.Leu548=
ENST00000638709.2:c.472C= ENSP00000491912.2:p.Leu158=
ENST00000682296.1:n.990C=
ENST00000682550.1:c.1297C= ENSP00000507633.1:p.Leu433=
ENST00000682772.1:c.472C= ENSP00000506848.1:p.Leu158=
ENST00000682904.1:n.468C=
ENST00000683211.1:c.1642C= ENSP00000508257.1:p.Leu548=
ENST00000683250.1:c.*350C= ENSP00000506847.1:n.*350C=
ENST00000683418.1:n.3989C=
ENST00000684153.1:c.1297C= ENSP00000506937.1:p.Leu433=
ENST00000684516.1:n.2661C=
ENST00000358487.10:c.1648C= MANE Select ENSP00000351276.6:p.Leu550=
ENST00000336553.10:c.1375C= ENSP00000337665.6:p.Leu459=
ENST00000346997.6:c.1642C= ENSP00000263451.5:p.Leu548=
ENST00000351936.10:c.1648C= ENSP00000309878.9:p.Leu550=
ENST00000356226.8:c.1297C= ENSP00000348559.4:p.Leu433=
ENST00000357555.9:c.1381C= ENSP00000350166.5:p.Leu461=
ENST00000358487.9:c.1648C= ENSP00000351276.5:p.Leu550=
ENST00000360144.7:c.1384C= ENSP00000353262.3:p.Leu462=
ENST00000369056.5:c.1651C= ENSP00000358052.1:p.Leu551=
ENST00000369058.7:c.1651C= ENSP00000358054.3:p.Leu551=
ENST00000369059.5:c.1306C= ENSP00000358055.1:p.Leu436=
ENST00000369060.8:c.1300C= ENSP00000358056.4:p.Leu434=
ENST00000369061.8:c.1312C= ENSP00000358057.4:p.Leu438=
ENST00000429361.5:c.424C= ENSP00000404219.1:p.Leu142=
ENST00000457416.6:c.1651C= ENSP00000410294.2:p.Leu551=
ENST00000478859.5:c.964C= ENSP00000474011.1:p.Leu322=
ENST00000604236.5:c.*695C= ENSP00000474109.1:n.*695C=
ENST00000613048.4:c.1381C= ENSP00000484154.1:p.Leu461=
NM_000141.4:c.1648C= NP_000132.3:p.Leu550=
NM_001144913.1:c.1651C= NP_001138385.1:p.Leu551=
NM_001144914.1:c.1312C= NP_001138386.1:p.Leu438=
NM_001144915.1:c.1381C= NP_001138387.1:p.Leu461=
NM_001144916.1:c.1303C= NP_001138388.1:p.Leu435=
NM_001144917.1:c.1300C= NP_001138389.1:p.Leu434=
NM_001144918.1:c.1297C= NP_001138390.1:p.Leu433=
NM_001144919.1:c.1384C= NP_001138391.1:p.Leu462=
NM_022970.3:c.1651C= NP_075259.4:p.Leu551=
NM_023029.2:c.1381C= NP_075418.1:p.Leu461=
NR_073009.1:n.2098C=
XM_006717708.2:c.1702C= XP_006717771.1:p.Leu568=
XM_006717709.2:c.1699C= XP_006717772.1:p.Leu567=
XM_006717710.2:c.1708C= XP_006717773.1:p.Leu570=
XM_006717711.2:c.1441C= XP_006717774.1:p.Leu481=
XM_006717712.2:c.1363C= XP_006717775.1:p.Leu455=
XM_006717713.2:c.1705C= XP_006717776.1:p.Leu569=
XM_011539510.1:c.964C= XP_011537812.1:p.Leu322=
NM_001320654.1:c.964C= NP_001307583.1:p.Leu322=
NM_001320658.1:c.1642C= NP_001307587.1:p.Leu548=
XM_006717708.3:c.1702C= XP_006717771.1:p.Leu568=
XM_006717710.4:c.1708C= XP_006717773.1:p.Leu570=
XM_017015920.2:c.1702C= XP_016871409.1:p.Leu568=
XM_017015921.2:c.1699C= XP_016871410.1:p.Leu567=
XM_017015924.2:c.1360C= XP_016871413.1:p.Leu454=
XM_017015925.2:c.1354C= XP_016871414.1:p.Leu452=
XM_024447887.1:c.1438C= XP_024303655.1:p.Leu480=
XM_024447888.1:c.1435C= XP_024303656.1:p.Leu479=
XM_024447889.1:c.1432C= XP_024303657.1:p.Leu478=
XM_024447890.1:c.1441C= XP_024303658.1:p.Leu481=
XM_024447891.1:c.1363C= XP_024303659.1:p.Leu455=
XM_024447892.1:c.478C= XP_024303660.1:p.Leu160=
NM_000141.5:c.1648C= MANE Select NP_000132.3:p.Leu550=
NM_001144917.2:c.1300C= NP_001138389.1:p.Leu434=
NM_001144918.2:c.1297C= NP_001138390.1:p.Leu433=
NM_001144919.2:c.1384C= NP_001138391.1:p.Leu462=
NM_001320658.2:c.1642C= NP_001307587.1:p.Leu548=
NR_073009.2:n.2084C=
NM_001144915.2:c.1381C= NP_001138387.1:p.Leu461=
NM_001144916.2:c.1303C= NP_001138388.1:p.Leu435=
NM_001320654.2:c.964C= NP_001307583.1:p.Leu322=