Canonical Allele Identifier: CA645568650
Gene: FGFR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517386_121517392del , CM000672.2:g.121517386_121517392del GRCh38
NC_000010.10:g.123276900_123276906del , CM000672.1:g.123276900_123276906del GRCh37
NC_000010.9:g.123266890_123266896del NCBI36
NG_012449.1:g.86068_86074del
NG_012449.2:g.86068_86074del

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1087+1291_1087+1297del MANE Plus Clinical ENSP00000410294.2:n.1087+1291_1087+1297de...
ENST00000351936.11:c.1012_1018del ENSP00000309878.10:p.Gly338IlefsTer18
ENST00000638709.2:c.-159_-153del ENSP00000491912.2:n.-159_-153del
ENST00000682296.1:n.360_366del
ENST00000682400.1:n.667_673del
ENST00000682550.1:c.667_673del ENSP00000507633.1:p.Gly223IlefsTer18
ENST00000682772.1:c.-159_-153del ENSP00000506848.1:n.-159_-153del
ENST00000683211.1:c.1012_1018del ENSP00000508257.1:p.Gly338IlefsTer18
ENST00000683250.1:c.404-13450_404-13444del ENSP00000506847.1:n.404-13450_404-13444de...
ENST00000683418.1:n.3359_3365del
ENST00000683678.1:n.1012_1018del
ENST00000684153.1:c.667_673del ENSP00000506937.1:p.Gly223IlefsTer18
ENST00000358487.10:c.1012_1018del MANE Select ENSP00000351276.6:p.Gly338IlefsTer18
ENST00000336553.10:c.745_751del ENSP00000337665.6:p.Gly249IlefsTer18
ENST00000346997.6:c.1012_1018del ENSP00000263451.5:p.Gly338IlefsTer18
ENST00000351936.10:c.1018_1024del ENSP00000309878.9:p.Gly340IlefsTer18
ENST00000356226.8:c.667_673del ENSP00000348559.4:p.Gly223IlefsTer18
ENST00000357555.9:c.745_751del ENSP00000350166.5:p.Gly249IlefsTer18
ENST00000358487.9:c.1012_1018del ENSP00000351276.5:p.Gly338IlefsTer18
ENST00000360144.7:c.820+1291_820+1297del ENSP00000353262.3:n.820+1291_820+1297del
ENST00000369056.5:c.1087+1291_1087+1297del ENSP00000358052.1:n.1087+1291_1087+1297de...
ENST00000369058.7:c.1087+1291_1087+1297del ENSP00000358054.3:n.1087+1291_1087+1297de...
ENST00000369059.5:c.742+1291_742+1297del ENSP00000358055.1:n.742+1291_742+1297del
ENST00000369060.8:c.939+2588_939+2594del ENSP00000358056.4:n.939+2588_939+2594del
ENST00000369061.8:c.749-2072_749-2066del ENSP00000358057.4:n.749-2072_749-2066del
ENST00000457416.6:c.1087+1291_1087+1297del ENSP00000410294.2:n.1087+1291_1087+1297de...
ENST00000463870.5:n.221_227del
ENST00000478859.5:c.328_334del ENSP00000474011.1:p.Gly110IlefsTer18
ENST00000490349.5:n.1421_1427del
ENST00000604236.5:c.*59_*65del ENSP00000474109.1:n.*59_*65del
ENST00000613048.4:c.745_751del ENSP00000484154.1:p.Gly249IlefsTer18
NM_000141.4:c.1012_1018del NP_000132.3:p.Gly338IlefsTer18
NM_001144913.1:c.1087+1291_1087+1297del NP_001138385.1:n.1087+1291_1087+1297del
NM_001144914.1:c.749-2072_749-2066del NP_001138386.1:n.749-2072_749-2066del
NM_001144915.1:c.745_751del NP_001138387.1:p.Gly249IlefsTer18
NM_001144916.1:c.667_673del NP_001138388.1:p.Gly223IlefsTer18
NM_001144917.1:c.939+2588_939+2594del NP_001138389.1:n.939+2588_939+2594del
NM_001144918.1:c.667_673del NP_001138390.1:p.Gly223IlefsTer18
NM_001144919.1:c.820+1291_820+1297del NP_001138391.1:n.820+1291_820+1297del
NM_022970.3:c.1087+1291_1087+1297del NP_075259.4:n.1087+1291_1087+1297del
NM_023029.2:c.745_751del NP_075418.1:p.Gly249IlefsTer18
NR_073009.1:n.1462_1468del
XM_006717708.2:c.1144+1291_1144+1297del XP_006717771.1:n.1144+1291_1144+1297del
XM_006717709.2:c.1069_1075del XP_006717772.1:p.Gly357IlefsTer18
XM_006717710.2:c.1144+1291_1144+1297del XP_006717773.1:n.1144+1291_1144+1297del
XM_006717711.2:c.877+1291_877+1297del XP_006717774.1:n.877+1291_877+1297del
XM_006717712.2:c.799+1291_799+1297del XP_006717775.1:n.799+1291_799+1297del
XM_006717713.2:c.1069_1075del XP_006717776.1:p.Gly357IlefsTer18
XM_011539510.1:c.328_334del XP_011537812.1:p.Gly110IlefsTer18
NM_001320654.1:c.328_334del NP_001307583.1:p.Gly110IlefsTer18
NM_001320658.1:c.1012_1018del NP_001307587.1:p.Gly338IlefsTer18
XM_006717708.3:c.1144+1291_1144+1297del XP_006717771.1:n.1144+1291_1144+1297del
XM_006717710.4:c.1144+1291_1144+1297del XP_006717773.1:n.1144+1291_1144+1297del
XM_017015920.2:c.1144+1291_1144+1297del XP_016871409.1:n.1144+1291_1144+1297del
XM_017015921.2:c.1069_1075del XP_016871410.1:p.Gly357IlefsTer18
XM_017015924.2:c.724_730del XP_016871413.1:p.Gly242IlefsTer18
XM_017015925.2:c.724_730del XP_016871414.1:p.Gly242IlefsTer18
XM_024447887.1:c.802_808del XP_024303655.1:p.Gly268IlefsTer18
XM_024447888.1:c.877+1291_877+1297del XP_024303656.1:n.877+1291_877+1297del
XM_024447889.1:c.802_808del XP_024303657.1:p.Gly268IlefsTer18
XM_024447890.1:c.877+1291_877+1297del XP_024303658.1:n.877+1291_877+1297del
XM_024447891.1:c.799+1291_799+1297del XP_024303659.1:n.799+1291_799+1297del
XM_024447892.1:c.-159_-153del XP_024303660.1:n.-159_-153del
NM_000141.5:c.1012_1018del MANE Select NP_000132.3:p.Gly338IlefsTer18
NM_001144917.2:c.939+2588_939+2594del NP_001138389.1:n.939+2588_939+2594del
NM_001144918.2:c.667_673del NP_001138390.1:p.Gly223IlefsTer18
NM_001144919.2:c.820+1291_820+1297del NP_001138391.1:n.820+1291_820+1297del
NM_001320658.2:c.1012_1018del NP_001307587.1:p.Gly338IlefsTer18
NR_073009.2:n.1448_1454del
NM_001144915.2:c.745_751del NP_001138387.1:p.Gly249IlefsTer18
NM_001144916.2:c.667_673del NP_001138388.1:p.Gly223IlefsTer18
NM_001320654.2:c.328_334del NP_001307583.1:p.Gly110IlefsTer18