Canonical Allele Identifier: CA1941024614
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517394C= , CM000672.2:g.121517394C= GRCh38
NC_000010.10:g.123276908C= , CM000672.1:g.123276908C= GRCh37
NC_000010.9:g.123266898C= NCBI36
NG_012449.1:g.86065G=
NG_012449.2:g.86065G=

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1288G= MANE Plus Clinical ENSP00000410294.2:n.1087+1288G=
ENST00000351936.11:c.1009G= ENSP00000309878.10:p.Ala337=
ENST00000638709.2:c.-162G= ENSP00000491912.2:n.-162G=
ENST00000682296.1:n.357G=
ENST00000682400.1:n.664G=
ENST00000682550.1:c.664G= ENSP00000507633.1:p.Ala222=
ENST00000682772.1:c.-162G= ENSP00000506848.1:n.-162G=
ENST00000683211.1:c.1009G= ENSP00000508257.1:p.Ala337=
ENST00000683250.1:c.404-13453G= ENSP00000506847.1:n.404-13453G=
ENST00000683418.1:n.3356G=
ENST00000683678.1:n.1009G=
ENST00000684153.1:c.664G= ENSP00000506937.1:p.Ala222=
ENST00000358487.10:c.1009G= MANE Select ENSP00000351276.6:p.Ala337=
ENST00000336553.10:c.742G= ENSP00000337665.6:p.Ala248=
ENST00000346997.6:c.1009G= ENSP00000263451.5:p.Ala337=
ENST00000351936.10:c.1015G= ENSP00000309878.9:p.Ala339=
ENST00000356226.8:c.664G= ENSP00000348559.4:p.Ala222=
ENST00000357555.9:c.742G= ENSP00000350166.5:p.Ala248=
ENST00000358487.9:c.1009G= ENSP00000351276.5:p.Ala337=
ENST00000360144.7:c.820+1288G= ENSP00000353262.3:n.820+1288G=
ENST00000369056.5:c.1087+1288G= ENSP00000358052.1:n.1087+1288G=
ENST00000369058.7:c.1087+1288G= ENSP00000358054.3:n.1087+1288G=
ENST00000369059.5:c.742+1288G= ENSP00000358055.1:n.742+1288G=
ENST00000369060.8:c.939+2585G= ENSP00000358056.4:n.939+2585G=
ENST00000369061.8:c.749-2075G= ENSP00000358057.4:n.749-2075G=
ENST00000457416.6:c.1087+1288G= ENSP00000410294.2:n.1087+1288G=
ENST00000463870.5:n.218G=
ENST00000478859.5:c.325G= ENSP00000474011.1:p.Ala109=
ENST00000490349.5:n.1418G=
ENST00000604236.5:c.*56G= ENSP00000474109.1:n.*56G=
ENST00000613048.4:c.742G= ENSP00000484154.1:p.Ala248=
NM_000141.4:c.1009G= NP_000132.3:p.Ala337=
NM_001144913.1:c.1087+1288G= NP_001138385.1:n.1087+1288G=
NM_001144914.1:c.749-2075G= NP_001138386.1:n.749-2075G=
NM_001144915.1:c.742G= NP_001138387.1:p.Ala248=
NM_001144916.1:c.664G= NP_001138388.1:p.Ala222=
NM_001144917.1:c.939+2585G= NP_001138389.1:n.939+2585G=
NM_001144918.1:c.664G= NP_001138390.1:p.Ala222=
NM_001144919.1:c.820+1288G= NP_001138391.1:n.820+1288G=
NM_022970.3:c.1087+1288G= NP_075259.4:n.1087+1288G=
NM_023029.2:c.742G= NP_075418.1:p.Ala248=
NR_073009.1:n.1459G=
XM_006717708.2:c.1144+1288G= XP_006717771.1:n.1144+1288G=
XM_006717709.2:c.1066G= XP_006717772.1:p.Ala356=
XM_006717710.2:c.1144+1288G= XP_006717773.1:n.1144+1288G=
XM_006717711.2:c.877+1288G= XP_006717774.1:n.877+1288G=
XM_006717712.2:c.799+1288G= XP_006717775.1:n.799+1288G=
XM_006717713.2:c.1066G= XP_006717776.1:p.Ala356=
XM_011539510.1:c.325G= XP_011537812.1:p.Ala109=
NM_001320654.1:c.325G= NP_001307583.1:p.Ala109=
NM_001320658.1:c.1009G= NP_001307587.1:p.Ala337=
XM_006717708.3:c.1144+1288G= XP_006717771.1:n.1144+1288G=
XM_006717710.4:c.1144+1288G= XP_006717773.1:n.1144+1288G=
XM_017015920.2:c.1144+1288G= XP_016871409.1:n.1144+1288G=
XM_017015921.2:c.1066G= XP_016871410.1:p.Ala356=
XM_017015924.2:c.721G= XP_016871413.1:p.Ala241=
XM_017015925.2:c.721G= XP_016871414.1:p.Ala241=
XM_024447887.1:c.799G= XP_024303655.1:p.Ala267=
XM_024447888.1:c.877+1288G= XP_024303656.1:n.877+1288G=
XM_024447889.1:c.799G= XP_024303657.1:p.Ala267=
XM_024447890.1:c.877+1288G= XP_024303658.1:n.877+1288G=
XM_024447891.1:c.799+1288G= XP_024303659.1:n.799+1288G=
XM_024447892.1:c.-162G= XP_024303660.1:n.-162G=
NM_000141.5:c.1009G= MANE Select NP_000132.3:p.Ala337=
NM_001144917.2:c.939+2585G= NP_001138389.1:n.939+2585G=
NM_001144918.2:c.664G= NP_001138390.1:p.Ala222=
NM_001144919.2:c.820+1288G= NP_001138391.1:n.820+1288G=
NM_001320658.2:c.1009G= NP_001307587.1:p.Ala337=
NR_073009.2:n.1445G=
NM_001144915.2:c.742G= NP_001138387.1:p.Ala248=
NM_001144916.2:c.664G= NP_001138388.1:p.Ala222=
NM_001320654.2:c.325G= NP_001307583.1:p.Ala109=