Canonical Allele Identifier: CA1941024607
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517386T= , CM000672.2:g.121517386T= GRCh38
NC_000010.10:g.123276900T= , CM000672.1:g.123276900T= GRCh37
NC_000010.9:g.123266890T= NCBI36
NG_012449.1:g.86073A=
NG_012449.2:g.86073A=

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1296A= MANE Plus Clinical ENSP00000410294.2:n.1087+1296A=
ENST00000351936.11:c.1017A= ENSP00000309878.10:p.Glu339=
ENST00000638709.2:c.-154A= ENSP00000491912.2:n.-154A=
ENST00000682296.1:n.365A=
ENST00000682400.1:n.672A=
ENST00000682550.1:c.672A= ENSP00000507633.1:p.Glu224=
ENST00000682772.1:c.-154A= ENSP00000506848.1:n.-154A=
ENST00000683211.1:c.1017A= ENSP00000508257.1:p.Glu339=
ENST00000683250.1:c.404-13445A= ENSP00000506847.1:n.404-13445A=
ENST00000683418.1:n.3364A=
ENST00000683678.1:n.1017A=
ENST00000684153.1:c.672A= ENSP00000506937.1:p.Glu224=
ENST00000358487.10:c.1017A= MANE Select ENSP00000351276.6:p.Glu339=
ENST00000336553.10:c.750A= ENSP00000337665.6:p.Glu250=
ENST00000346997.6:c.1017A= ENSP00000263451.5:p.Glu339=
ENST00000351936.10:c.1023A= ENSP00000309878.9:p.Glu341=
ENST00000356226.8:c.672A= ENSP00000348559.4:p.Glu224=
ENST00000357555.9:c.750A= ENSP00000350166.5:p.Glu250=
ENST00000358487.9:c.1017A= ENSP00000351276.5:p.Glu339=
ENST00000360144.7:c.820+1296A= ENSP00000353262.3:n.820+1296A=
ENST00000369056.5:c.1087+1296A= ENSP00000358052.1:n.1087+1296A=
ENST00000369058.7:c.1087+1296A= ENSP00000358054.3:n.1087+1296A=
ENST00000369059.5:c.742+1296A= ENSP00000358055.1:n.742+1296A=
ENST00000369060.8:c.939+2593A= ENSP00000358056.4:n.939+2593A=
ENST00000369061.8:c.749-2067A= ENSP00000358057.4:n.749-2067A=
ENST00000457416.6:c.1087+1296A= ENSP00000410294.2:n.1087+1296A=
ENST00000463870.5:n.226A=
ENST00000478859.5:c.333A= ENSP00000474011.1:p.Glu111=
ENST00000490349.5:n.1426A=
ENST00000604236.5:c.*64A= ENSP00000474109.1:n.*64A=
ENST00000613048.4:c.750A= ENSP00000484154.1:p.Glu250=
NM_000141.4:c.1017A= NP_000132.3:p.Glu339=
NM_001144913.1:c.1087+1296A= NP_001138385.1:n.1087+1296A=
NM_001144914.1:c.749-2067A= NP_001138386.1:n.749-2067A=
NM_001144915.1:c.750A= NP_001138387.1:p.Glu250=
NM_001144916.1:c.672A= NP_001138388.1:p.Glu224=
NM_001144917.1:c.939+2593A= NP_001138389.1:n.939+2593A=
NM_001144918.1:c.672A= NP_001138390.1:p.Glu224=
NM_001144919.1:c.820+1296A= NP_001138391.1:n.820+1296A=
NM_022970.3:c.1087+1296A= NP_075259.4:n.1087+1296A=
NM_023029.2:c.750A= NP_075418.1:p.Glu250=
NR_073009.1:n.1467A=
XM_006717708.2:c.1144+1296A= XP_006717771.1:n.1144+1296A=
XM_006717709.2:c.1074A= XP_006717772.1:p.Glu358=
XM_006717710.2:c.1144+1296A= XP_006717773.1:n.1144+1296A=
XM_006717711.2:c.877+1296A= XP_006717774.1:n.877+1296A=
XM_006717712.2:c.799+1296A= XP_006717775.1:n.799+1296A=
XM_006717713.2:c.1074A= XP_006717776.1:p.Glu358=
XM_011539510.1:c.333A= XP_011537812.1:p.Glu111=
NM_001320654.1:c.333A= NP_001307583.1:p.Glu111=
NM_001320658.1:c.1017A= NP_001307587.1:p.Glu339=
XM_006717708.3:c.1144+1296A= XP_006717771.1:n.1144+1296A=
XM_006717710.4:c.1144+1296A= XP_006717773.1:n.1144+1296A=
XM_017015920.2:c.1144+1296A= XP_016871409.1:n.1144+1296A=
XM_017015921.2:c.1074A= XP_016871410.1:p.Glu358=
XM_017015924.2:c.729A= XP_016871413.1:p.Glu243=
XM_017015925.2:c.729A= XP_016871414.1:p.Glu243=
XM_024447887.1:c.807A= XP_024303655.1:p.Glu269=
XM_024447888.1:c.877+1296A= XP_024303656.1:n.877+1296A=
XM_024447889.1:c.807A= XP_024303657.1:p.Glu269=
XM_024447890.1:c.877+1296A= XP_024303658.1:n.877+1296A=
XM_024447891.1:c.799+1296A= XP_024303659.1:n.799+1296A=
XM_024447892.1:c.-154A= XP_024303660.1:n.-154A=
NM_000141.5:c.1017A= MANE Select NP_000132.3:p.Glu339=
NM_001144917.2:c.939+2593A= NP_001138389.1:n.939+2593A=
NM_001144918.2:c.672A= NP_001138390.1:p.Glu224=
NM_001144919.2:c.820+1296A= NP_001138391.1:n.820+1296A=
NM_001320658.2:c.1017A= NP_001307587.1:p.Glu339=
NR_073009.2:n.1453A=
NM_001144915.2:c.750A= NP_001138387.1:p.Glu250=
NM_001144916.2:c.672A= NP_001138388.1:p.Glu224=
NM_001320654.2:c.333A= NP_001307583.1:p.Glu111=