Canonical Allele Identifier: CA1941024611
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517390_121517391delinsCC , CM000672.2:g.121517390_121517391delinsCC GRCh38
NC_000010.10:g.123276904_123276905delinsCC , CM000672.1:g.123276904_123276905delinsCC GRCh37
NC_000010.9:g.123266894_123266895delinsCC NCBI36
NG_012449.1:g.86068_86069delinsGG
NG_012449.2:g.86068_86069delinsGG

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1291_1087+1292delinsGG MANE Plus Clinical ENSP00000410294.2:n.1087+1291_1087+1292de...
ENST00000351936.11:c.1012_1013delinsGG ENSP00000309878.10:p.Gly338=
ENST00000638709.2:c.-159_-158delinsGG ENSP00000491912.2:n.-159_-158delinsGG
ENST00000682296.1:n.360_361delinsGG
ENST00000682400.1:n.667_668delinsGG
ENST00000682550.1:c.667_668delinsGG ENSP00000507633.1:p.Gly223=
ENST00000682772.1:c.-159_-158delinsGG ENSP00000506848.1:n.-159_-158delinsGG
ENST00000683211.1:c.1012_1013delinsGG ENSP00000508257.1:p.Gly338=
ENST00000683250.1:c.404-13450_404-13449delinsGG ENSP00000506847.1:n.404-13450_404-13449de...
ENST00000683418.1:n.3359_3360delinsGG
ENST00000683678.1:n.1012_1013delinsGG
ENST00000684153.1:c.667_668delinsGG ENSP00000506937.1:p.Gly223=
ENST00000358487.10:c.1012_1013delinsGG MANE Select ENSP00000351276.6:p.Gly338=
ENST00000336553.10:c.745_746delinsGG ENSP00000337665.6:p.Gly249=
ENST00000346997.6:c.1012_1013delinsGG ENSP00000263451.5:p.Gly338=
ENST00000351936.10:c.1018_1019delinsGG ENSP00000309878.9:p.Gly340=
ENST00000356226.8:c.667_668delinsGG ENSP00000348559.4:p.Gly223=
ENST00000357555.9:c.745_746delinsGG ENSP00000350166.5:p.Gly249=
ENST00000358487.9:c.1012_1013delinsGG ENSP00000351276.5:p.Gly338=
ENST00000360144.7:c.820+1291_820+1292delinsGG ENSP00000353262.3:n.820+1291_820+1292deli...
ENST00000369056.5:c.1087+1291_1087+1292delinsGG ENSP00000358052.1:n.1087+1291_1087+1292de...
ENST00000369058.7:c.1087+1291_1087+1292delinsGG ENSP00000358054.3:n.1087+1291_1087+1292de...
ENST00000369059.5:c.742+1291_742+1292delinsGG ENSP00000358055.1:n.742+1291_742+1292deli...
ENST00000369060.8:c.939+2588_939+2589delinsGG ENSP00000358056.4:n.939+2588_939+2589deli...
ENST00000369061.8:c.749-2072_749-2071delinsGG ENSP00000358057.4:n.749-2072_749-2071deli...
ENST00000457416.6:c.1087+1291_1087+1292delinsGG ENSP00000410294.2:n.1087+1291_1087+1292de...
ENST00000463870.5:n.221_222delinsGG
ENST00000478859.5:c.328_329delinsGG ENSP00000474011.1:p.Gly110=
ENST00000490349.5:n.1421_1422delinsGG
ENST00000604236.5:c.*59_*60delinsGG ENSP00000474109.1:n.*59_*60delinsGG
ENST00000613048.4:c.745_746delinsGG ENSP00000484154.1:p.Gly249=
NM_000141.4:c.1012_1013delinsGG NP_000132.3:p.Gly338=
NM_001144913.1:c.1087+1291_1087+1292delinsGG NP_001138385.1:n.1087+1291_1087+1292delin...
NM_001144914.1:c.749-2072_749-2071delinsGG NP_001138386.1:n.749-2072_749-2071delinsG...
NM_001144915.1:c.745_746delinsGG NP_001138387.1:p.Gly249=
NM_001144916.1:c.667_668delinsGG NP_001138388.1:p.Gly223=
NM_001144917.1:c.939+2588_939+2589delinsGG NP_001138389.1:n.939+2588_939+2589delinsG...
NM_001144918.1:c.667_668delinsGG NP_001138390.1:p.Gly223=
NM_001144919.1:c.820+1291_820+1292delinsGG NP_001138391.1:n.820+1291_820+1292delinsG...
NM_022970.3:c.1087+1291_1087+1292delinsGG NP_075259.4:n.1087+1291_1087+1292delinsGG...
NM_023029.2:c.745_746delinsGG NP_075418.1:p.Gly249=
NR_073009.1:n.1462_1463delinsGG
XM_006717708.2:c.1144+1291_1144+1292delinsGG XP_006717771.1:n.1144+1291_1144+1292delin...
XM_006717709.2:c.1069_1070delinsGG XP_006717772.1:p.Gly357=
XM_006717710.2:c.1144+1291_1144+1292delinsGG XP_006717773.1:n.1144+1291_1144+1292delin...
XM_006717711.2:c.877+1291_877+1292delinsGG XP_006717774.1:n.877+1291_877+1292delinsG...
XM_006717712.2:c.799+1291_799+1292delinsGG XP_006717775.1:n.799+1291_799+1292delinsG...
XM_006717713.2:c.1069_1070delinsGG XP_006717776.1:p.Gly357=
XM_011539510.1:c.328_329delinsGG XP_011537812.1:p.Gly110=
NM_001320654.1:c.328_329delinsGG NP_001307583.1:p.Gly110=
NM_001320658.1:c.1012_1013delinsGG NP_001307587.1:p.Gly338=
XM_006717708.3:c.1144+1291_1144+1292delinsGG XP_006717771.1:n.1144+1291_1144+1292delin...
XM_006717710.4:c.1144+1291_1144+1292delinsGG XP_006717773.1:n.1144+1291_1144+1292delin...
XM_017015920.2:c.1144+1291_1144+1292delinsGG XP_016871409.1:n.1144+1291_1144+1292delin...
XM_017015921.2:c.1069_1070delinsGG XP_016871410.1:p.Gly357=
XM_017015924.2:c.724_725delinsGG XP_016871413.1:p.Gly242=
XM_017015925.2:c.724_725delinsGG XP_016871414.1:p.Gly242=
XM_024447887.1:c.802_803delinsGG XP_024303655.1:p.Gly268=
XM_024447888.1:c.877+1291_877+1292delinsGG XP_024303656.1:n.877+1291_877+1292delinsG...
XM_024447889.1:c.802_803delinsGG XP_024303657.1:p.Gly268=
XM_024447890.1:c.877+1291_877+1292delinsGG XP_024303658.1:n.877+1291_877+1292delinsG...
XM_024447891.1:c.799+1291_799+1292delinsGG XP_024303659.1:n.799+1291_799+1292delinsG...
XM_024447892.1:c.-159_-158delinsGG XP_024303660.1:n.-159_-158delinsGG
NM_000141.5:c.1012_1013delinsGG MANE Select NP_000132.3:p.Gly338=
NM_001144917.2:c.939+2588_939+2589delinsGG NP_001138389.1:n.939+2588_939+2589delinsG...
NM_001144918.2:c.667_668delinsGG NP_001138390.1:p.Gly223=
NM_001144919.2:c.820+1291_820+1292delinsGG NP_001138391.1:n.820+1291_820+1292delinsG...
NM_001320658.2:c.1012_1013delinsGG NP_001307587.1:p.Gly338=
NR_073009.2:n.1448_1449delinsGG
NM_001144915.2:c.745_746delinsGG NP_001138387.1:p.Gly249=
NM_001144916.2:c.667_668delinsGG NP_001138388.1:p.Gly223=
NM_001320654.2:c.328_329delinsGG NP_001307583.1:p.Gly110=