Canonical Allele Identifier: CA658658022
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 478044
ClinVar RCV Id: RCV000558696
dbSNP Id: rs1554928905

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517390_121517391delinsTT , CM000672.2:g.121517390_121517391delinsTT GRCh38
NC_000010.10:g.123276904_123276905delinsTT , CM000672.1:g.123276904_123276905delinsTT GRCh37
NC_000010.9:g.123266894_123266895delinsTT NCBI36
NG_012449.1:g.86068_86069delinsAA
NG_012449.2:g.86068_86069delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000358487.10:c.1012_1013delinsAA MANE Select ENSP00000351276.6:p.Gly338Lys
ENST00000336553.10:c.745_746delinsAA ENSP00000337665.6:p.Gly249Lys
ENST00000346997.6:c.1012_1013delinsAA ENSP00000263451.5:p.Gly338Lys
ENST00000351936.10:c.1018_1019delinsAA ENSP00000309878.9:p.Gly340Lys
ENST00000356226.8:c.667_668delinsAA ENSP00000348559.4:p.Gly223Lys
ENST00000357555.9:c.745_746delinsAA ENSP00000350166.5:p.Gly249Lys
ENST00000358487.9:c.1012_1013delinsAA ENSP00000351276.5:p.Gly338Lys
ENST00000360144.7:c.820+1291_820+1292delinsAA ENSP00000353262.3:p.=
ENST00000369056.5:c.1087+1291_1087+1292delinsAA ENSP00000358052.1:p.=
ENST00000369058.7:c.1087+1291_1087+1292delinsAA ENSP00000358054.3:p.=
ENST00000369059.5:c.742+1291_742+1292delinsAA ENSP00000358055.1:p.=
ENST00000369060.8:c.939+2588_939+2589delinsAA ENSP00000358056.4:p.=
ENST00000369061.8:c.749-2072_749-2071delinsAA ENSP00000358057.4:p.=
ENST00000457416.6:c.1087+1291_1087+1292delinsAA ENSP00000410294.2:p.=
ENST00000463870.5:n.221_222delinsAA
ENST00000478859.5:c.328_329delinsAA ENSP00000474011.1:p.Gly110Lys
ENST00000490349.5:n.1421_1422delinsAA
ENST00000604236.5:c.*59_*60delinsAA ENSP00000474109.1:p.=
ENST00000613048.4:c.745_746delinsAA ENSP00000484154.1:p.Gly249Lys
NM_000141.4:c.1012_1013delinsAA NP_000132.3:p.Gly338Lys
NM_001144913.1:c.1087+1291_1087+1292delinsAA NP_001138385.1:p.=
NM_001144914.1:c.749-2072_749-2071delinsAA NP_001138386.1:p.=
NM_001144915.1:c.745_746delinsAA NP_001138387.1:p.Gly249Lys
NM_001144916.1:c.667_668delinsAA NP_001138388.1:p.Gly223Lys
NM_001144917.1:c.939+2588_939+2589delinsAA NP_001138389.1:p.=
NM_001144918.1:c.667_668delinsAA NP_001138390.1:p.Gly223Lys
NM_001144919.1:c.820+1291_820+1292delinsAA NP_001138391.1:p.=
NM_022970.3:c.1087+1291_1087+1292delinsAA NP_075259.4:p.=
NM_023029.2:c.745_746delinsAA NP_075418.1:p.Gly249Lys
NR_073009.1:n.1462_1463delinsAA
XM_006717708.2:c.1144+1291_1144+1292delinsAA XP_006717771.1:p.=
XM_006717709.2:c.1069_1070delinsAA XP_006717772.1:p.Gly357Lys
XM_006717710.2:c.1144+1291_1144+1292delinsAA XP_006717773.1:p.=
XM_006717711.2:c.877+1291_877+1292delinsAA XP_006717774.1:p.=
XM_006717712.2:c.799+1291_799+1292delinsAA XP_006717775.1:p.=
XM_006717713.2:c.1069_1070delinsAA XP_006717776.1:p.Gly357Lys
XM_011539510.1:c.328_329delinsAA XP_011537812.1:p.Gly110Lys
NM_001320654.1:c.328_329delinsAA NP_001307583.1:p.Gly110Lys
NM_001320658.1:c.1012_1013delinsAA NP_001307587.1:p.Gly338Lys
XM_006717708.3:c.1144+1291_1144+1292delinsAA XP_006717771.1:p.=
XM_006717710.4:c.1144+1291_1144+1292delinsAA XP_006717773.1:p.=
XM_017015920.2:c.1144+1291_1144+1292delinsAA XP_016871409.1:p.=
XM_017015921.2:c.1069_1070delinsAA XP_016871410.1:p.Gly357Lys
XM_017015924.2:c.724_725delinsAA XP_016871413.1:p.Gly242Lys
XM_017015925.2:c.724_725delinsAA XP_016871414.1:p.Gly242Lys
XM_024447887.1:c.802_803delinsAA XP_024303655.1:p.Gly268Lys
XM_024447888.1:c.877+1291_877+1292delinsAA XP_024303656.1:p.=
XM_024447889.1:c.802_803delinsAA XP_024303657.1:p.Gly268Lys
XM_024447890.1:c.877+1291_877+1292delinsAA XP_024303658.1:p.=
XM_024447891.1:c.799+1291_799+1292delinsAA XP_024303659.1:p.=
XM_024447892.1:c.-159_-158delinsAA XP_024303660.1:p.=
NM_000141.5:c.1012_1013delinsAA MANE Select NP_000132.3:p.Gly338Lys
NM_001144917.2:c.939+2588_939+2589delinsAA NP_001138389.1:p.=
NM_001144918.2:c.667_668delinsAA NP_001138390.1:p.Gly223Lys
NM_001144919.2:c.820+1291_820+1292delinsAA NP_001138391.1:p.=
NM_001320658.2:c.1012_1013delinsAA NP_001307587.1:p.Gly338Lys
NR_073009.2:n.1448_1449delinsAA
NM_001144915.2:c.745_746delinsAA NP_001138387.1:p.Gly249Lys
NM_001144916.2:c.667_668delinsAA NP_001138388.1:p.Gly223Lys
NM_001320654.2:c.328_329delinsAA NP_001307583.1:p.Gly110Lys