Canonical Allele Identifier: CA1941016791
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121496705C= , CM000672.2:g.121496705C= GRCh38
NC_000010.10:g.123256219C= , CM000672.1:g.123256219C= GRCh37
NC_000010.9:g.123246209C= NCBI36
NG_012449.1:g.106754G=
NG_012449.2:g.106754G=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1690G= MANE Select NP_000132.3:p.Val564=
ENST00000358487.10:c.1690G= MANE Select ENSP00000351276.6:p.Val564=
ENST00000457416.7:c.1693G= MANE Plus Clinical ENSP00000410294.2:p.Val565=
NM_000141.4:c.1690G= NP_000132.3:p.Val564=
NM_001144913.1:c.1693G= NP_001138385.1:p.Val565=
NM_001144914.1:c.1354G= NP_001138386.1:p.Val452=
NM_001144915.1:c.1423G= NP_001138387.1:p.Val475=
NM_001144915.2:c.1423G= NP_001138387.1:p.Val475=
NM_001144916.1:c.1345G= NP_001138388.1:p.Val449=
NM_001144916.2:c.1345G= NP_001138388.1:p.Val449=
NM_001144917.1:c.1342G= NP_001138389.1:p.Val448=
NM_001144917.2:c.1342G= NP_001138389.1:p.Val448=
NM_001144918.1:c.1339G= NP_001138390.1:p.Val447=
NM_001144918.2:c.1339G= NP_001138390.1:p.Val447=
NM_001144919.1:c.1426G= NP_001138391.1:p.Val476=
NM_001144919.2:c.1426G= NP_001138391.1:p.Val476=
NM_001320654.1:c.1006G= NP_001307583.1:p.Val336=
NM_001320654.2:c.1006G= NP_001307583.1:p.Val336=
NM_001320658.1:c.1684G= NP_001307587.1:p.Val562=
NM_001320658.2:c.1684G= NP_001307587.1:p.Val562=
NM_022970.3:c.1693G= NP_075259.4:p.Val565=
NM_023029.2:c.1423G= NP_075418.1:p.Val475=
NR_073009.1:n.2140G=
NR_073009.2:n.2126G=
ENST00000336553.10:c.1417G= ENSP00000337665.6:p.Val473=
ENST00000346997.6:c.1684G= ENSP00000263451.5:p.Val562=
ENST00000351936.10:c.1690G= ENSP00000309878.9:p.Val564=
ENST00000351936.11:c.1684G= ENSP00000309878.10:p.Val562=
ENST00000356226.8:c.1339G= ENSP00000348559.4:p.Val447=
ENST00000357555.9:c.1423G= ENSP00000350166.5:p.Val475=
ENST00000358487.9:c.1690G= ENSP00000351276.5:p.Val564=
ENST00000360144.7:c.1426G= ENSP00000353262.3:p.Val476=
ENST00000369056.5:c.1693G= ENSP00000358052.1:p.Val565=
ENST00000369058.7:c.1693G= ENSP00000358054.3:p.Val565=
ENST00000369059.5:c.1348G= ENSP00000358055.1:p.Val450=
ENST00000369060.8:c.1342G= ENSP00000358056.4:p.Val448=
ENST00000369061.8:c.1354G= ENSP00000358057.4:p.Val452=
ENST00000429361.5:c.466G= ENSP00000404219.1:p.Val156=
ENST00000457416.6:c.1693G= ENSP00000410294.2:p.Val565=
ENST00000478859.5:c.1006G= ENSP00000474011.1:p.Val336=
ENST00000604236.5:c.*737G= ENSP00000474109.1:n.*737G=
ENST00000613048.4:c.1423G= ENSP00000484154.1:p.Val475=
ENST00000638709.2:c.514G= ENSP00000491912.2:p.Val172=
ENST00000682296.1:n.1032G=
ENST00000682550.1:c.1339G= ENSP00000507633.1:p.Val447=
ENST00000682772.1:c.514G= ENSP00000506848.1:p.Val172=
ENST00000682904.1:n.510G=
ENST00000683029.1:n.102G=
ENST00000683211.1:c.1684G= ENSP00000508257.1:p.Val562=
ENST00000683250.1:c.*392G= ENSP00000506847.1:n.*392G=
ENST00000683418.1:n.4031G=
ENST00000684153.1:c.1339G= ENSP00000506937.1:p.Val447=
ENST00000684516.1:n.2703G=
XM_006717708.2:c.1744G= XP_006717771.1:p.Val582=
XM_006717708.3:c.1744G= XP_006717771.1:p.Val582=
XM_006717709.2:c.1741G= XP_006717772.1:p.Val581=
XM_006717710.2:c.1750G= XP_006717773.1:p.Val584=
XM_006717710.4:c.1750G= XP_006717773.1:p.Val584=
XM_006717711.2:c.1483G= XP_006717774.1:p.Val495=
XM_006717712.2:c.1405G= XP_006717775.1:p.Val469=
XM_006717713.2:c.1747G= XP_006717776.1:p.Val583=
XM_011539510.1:c.1006G= XP_011537812.1:p.Val336=
XM_017015920.2:c.1744G= XP_016871409.1:p.Val582=
XM_017015921.2:c.1741G= XP_016871410.1:p.Val581=
XM_017015924.2:c.1402G= XP_016871413.1:p.Val468=
XM_017015925.2:c.1396G= XP_016871414.1:p.Val466=
XM_024447887.1:c.1480G= XP_024303655.1:p.Val494=
XM_024447888.1:c.1477G= XP_024303656.1:p.Val493=
XM_024447889.1:c.1474G= XP_024303657.1:p.Val492=
XM_024447890.1:c.1483G= XP_024303658.1:p.Val495=
XM_024447891.1:c.1405G= XP_024303659.1:p.Val469=
XM_024447892.1:c.520G= XP_024303660.1:p.Val174=