Canonical Allele Identifier: CA1941017706
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498528T= , CM000672.2:g.121498528T= GRCh38
NC_000010.10:g.123258042T= , CM000672.1:g.123258042T= GRCh37
NC_000010.9:g.123248032T= NCBI36
NG_012449.1:g.104931A=
NG_012449.2:g.104931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1642A= MANE Plus Clinical ENSP00000410294.2:p.Ile548=
ENST00000351936.11:c.1633A= ENSP00000309878.10:p.Ile545=
ENST00000638709.2:c.463A= ENSP00000491912.2:p.Ile155=
ENST00000682296.1:n.981A=
ENST00000682550.1:c.1288A= ENSP00000507633.1:p.Ile430=
ENST00000682772.1:c.463A= ENSP00000506848.1:p.Ile155=
ENST00000682904.1:n.459A=
ENST00000683211.1:c.1633A= ENSP00000508257.1:p.Ile545=
ENST00000683250.1:c.*341A= ENSP00000506847.1:n.*341A=
ENST00000683418.1:n.3980A=
ENST00000684153.1:c.1288A= ENSP00000506937.1:p.Ile430=
ENST00000684516.1:n.2652A=
ENST00000358487.10:c.1639A= MANE Select ENSP00000351276.6:p.Ile547=
ENST00000336553.10:c.1366A= ENSP00000337665.6:p.Ile456=
ENST00000346997.6:c.1633A= ENSP00000263451.5:p.Ile545=
ENST00000351936.10:c.1639A= ENSP00000309878.9:p.Ile547=
ENST00000356226.8:c.1288A= ENSP00000348559.4:p.Ile430=
ENST00000357555.9:c.1372A= ENSP00000350166.5:p.Ile458=
ENST00000358487.9:c.1639A= ENSP00000351276.5:p.Ile547=
ENST00000360144.7:c.1375A= ENSP00000353262.3:p.Ile459=
ENST00000369056.5:c.1642A= ENSP00000358052.1:p.Ile548=
ENST00000369058.7:c.1642A= ENSP00000358054.3:p.Ile548=
ENST00000369059.5:c.1297A= ENSP00000358055.1:p.Ile433=
ENST00000369060.8:c.1291A= ENSP00000358056.4:p.Ile431=
ENST00000369061.8:c.1303A= ENSP00000358057.4:p.Ile435=
ENST00000429361.5:c.415A= ENSP00000404219.1:p.Ile139=
ENST00000457416.6:c.1642A= ENSP00000410294.2:p.Ile548=
ENST00000478859.5:c.955A= ENSP00000474011.1:p.Ile319=
ENST00000604236.5:c.*686A= ENSP00000474109.1:n.*686A=
ENST00000613048.4:c.1372A= ENSP00000484154.1:p.Ile458=
NM_000141.4:c.1639A= NP_000132.3:p.Ile547=
NM_001144913.1:c.1642A= NP_001138385.1:p.Ile548=
NM_001144914.1:c.1303A= NP_001138386.1:p.Ile435=
NM_001144915.1:c.1372A= NP_001138387.1:p.Ile458=
NM_001144916.1:c.1294A= NP_001138388.1:p.Ile432=
NM_001144917.1:c.1291A= NP_001138389.1:p.Ile431=
NM_001144918.1:c.1288A= NP_001138390.1:p.Ile430=
NM_001144919.1:c.1375A= NP_001138391.1:p.Ile459=
NM_022970.3:c.1642A= NP_075259.4:p.Ile548=
NM_023029.2:c.1372A= NP_075418.1:p.Ile458=
NR_073009.1:n.2089A=
XM_006717708.2:c.1693A= XP_006717771.1:p.Ile565=
XM_006717709.2:c.1690A= XP_006717772.1:p.Ile564=
XM_006717710.2:c.1699A= XP_006717773.1:p.Ile567=
XM_006717711.2:c.1432A= XP_006717774.1:p.Ile478=
XM_006717712.2:c.1354A= XP_006717775.1:p.Ile452=
XM_006717713.2:c.1696A= XP_006717776.1:p.Ile566=
XM_011539510.1:c.955A= XP_011537812.1:p.Ile319=
NM_001320654.1:c.955A= NP_001307583.1:p.Ile319=
NM_001320658.1:c.1633A= NP_001307587.1:p.Ile545=
XM_006717708.3:c.1693A= XP_006717771.1:p.Ile565=
XM_006717710.4:c.1699A= XP_006717773.1:p.Ile567=
XM_017015920.2:c.1693A= XP_016871409.1:p.Ile565=
XM_017015921.2:c.1690A= XP_016871410.1:p.Ile564=
XM_017015924.2:c.1351A= XP_016871413.1:p.Ile451=
XM_017015925.2:c.1345A= XP_016871414.1:p.Ile449=
XM_024447887.1:c.1429A= XP_024303655.1:p.Ile477=
XM_024447888.1:c.1426A= XP_024303656.1:p.Ile476=
XM_024447889.1:c.1423A= XP_024303657.1:p.Ile475=
XM_024447890.1:c.1432A= XP_024303658.1:p.Ile478=
XM_024447891.1:c.1354A= XP_024303659.1:p.Ile452=
XM_024447892.1:c.469A= XP_024303660.1:p.Ile157=
NM_000141.5:c.1639A= MANE Select NP_000132.3:p.Ile547=
NM_001144917.2:c.1291A= NP_001138389.1:p.Ile431=
NM_001144918.2:c.1288A= NP_001138390.1:p.Ile430=
NM_001144919.2:c.1375A= NP_001138391.1:p.Ile459=
NM_001320658.2:c.1633A= NP_001307587.1:p.Ile545=
NR_073009.2:n.2075A=
NM_001144915.2:c.1372A= NP_001138387.1:p.Ile458=
NM_001144916.2:c.1294A= NP_001138388.1:p.Ile432=
NM_001320654.2:c.955A= NP_001307583.1:p.Ile319=