Canonical Allele Identifier: CA2611199517
Gene: FGFR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121517345_121517346insTTTCAC , CM000672.2:g.121517345_121517346insTTTCAC GRCh38
NC_000010.10:g.123276859_123276860insTTTCAC , CM000672.1:g.123276859_123276860insTTTCAC GRCh37
NC_000010.9:g.123266849_123266850insTTTCAC NCBI36
NG_012449.1:g.86113_86114insGTGAAA
NG_012449.2:g.86113_86114insGTGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1087+1336_1087+1337insGTGAAA MANE Plus Clinical ENSP00000410294.2:n.1087+1336_1087+1337insGTGAAA
ENST00000351936.11:c.1057_1058insGTGAAA ENSP00000309878.10:p.His353delinsArgGluAsn
ENST00000638709.2:c.-114_-113insGTGAAA ENSP00000491912.2:n.-114_-113insGTGAAA
ENST00000682296.1:n.405_406insGTGAAA
ENST00000682400.1:n.712_713insGTGAAA
ENST00000682550.1:c.712_713insGTGAAA ENSP00000507633.1:p.His238delinsArgGluAsn
ENST00000682772.1:c.-114_-113insGTGAAA ENSP00000506848.1:n.-114_-113insGTGAAA
ENST00000683211.1:c.1057_1058insGTGAAA ENSP00000508257.1:p.His353delinsArgGluAsn
ENST00000683250.1:c.404-13405_404-13404insGTGAAA ENSP00000506847.1:n.404-13405_404-13404insGTGAAA
ENST00000683418.1:n.3404_3405insGTGAAA
ENST00000683678.1:n.1057_1058insGTGAAA
ENST00000684153.1:c.712_713insGTGAAA ENSP00000506937.1:p.His238delinsArgGluAsn
ENST00000358487.10:c.1057_1058insGTGAAA MANE Select ENSP00000351276.6:p.His353delinsArgGluAsn
ENST00000336553.10:c.790_791insGTGAAA ENSP00000337665.6:p.His264delinsArgGluAsn
ENST00000346997.6:c.1057_1058insGTGAAA ENSP00000263451.5:p.His353delinsArgGluAsn
ENST00000351936.10:c.1063_1064insGTGAAA ENSP00000309878.9:p.His355delinsArgGluAsn
ENST00000356226.8:c.712_713insGTGAAA ENSP00000348559.4:p.His238delinsArgGluAsn
ENST00000357555.9:c.790_791insGTGAAA ENSP00000350166.5:p.His264delinsArgGluAsn
ENST00000358487.9:c.1057_1058insGTGAAA ENSP00000351276.5:p.His353delinsArgGluAsn
ENST00000360144.7:c.820+1336_820+1337insGTGAAA ENSP00000353262.3:n.820+1336_820+1337insGTGAAA
ENST00000369056.5:c.1087+1336_1087+1337insGTGAAA ENSP00000358052.1:n.1087+1336_1087+1337insGTGAAA
ENST00000369058.7:c.1087+1336_1087+1337insGTGAAA ENSP00000358054.3:n.1087+1336_1087+1337insGTGAAA
ENST00000369059.5:c.742+1336_742+1337insGTGAAA ENSP00000358055.1:n.742+1336_742+1337insGTGAAA
ENST00000369060.8:c.939+2633_939+2634insGTGAAA ENSP00000358056.4:n.939+2633_939+2634insGTGAAA
ENST00000369061.8:c.749-2027_749-2026insGTGAAA ENSP00000358057.4:n.749-2027_749-2026insGTGAAA
ENST00000457416.6:c.1087+1336_1087+1337insGTGAAA ENSP00000410294.2:n.1087+1336_1087+1337insGTGAAA
ENST00000463870.5:n.266_267insGTGAAA
ENST00000478859.5:c.373_374insGTGAAA ENSP00000474011.1:p.His125delinsArgGluAsn
ENST00000490349.5:n.1466_1467insGTGAAA
ENST00000604236.5:c.*104_*105insGTGAAA ENSP00000474109.1:n.*104_*105insGTGAAA
ENST00000613048.4:c.790_791insGTGAAA ENSP00000484154.1:p.His264delinsArgGluAsn
NM_000141.4:c.1057_1058insGTGAAA NP_000132.3:p.His353delinsArgGluAsn
NM_001144913.1:c.1087+1336_1087+1337insGTGAAA NP_001138385.1:n.1087+1336_1087+1337insGTGAAA
NM_001144914.1:c.749-2027_749-2026insGTGAAA NP_001138386.1:n.749-2027_749-2026insGTGAAA
NM_001144915.1:c.790_791insGTGAAA NP_001138387.1:p.His264delinsArgGluAsn
NM_001144916.1:c.712_713insGTGAAA NP_001138388.1:p.His238delinsArgGluAsn
NM_001144917.1:c.939+2633_939+2634insGTGAAA NP_001138389.1:n.939+2633_939+2634insGTGAAA
NM_001144918.1:c.712_713insGTGAAA NP_001138390.1:p.His238delinsArgGluAsn
NM_001144919.1:c.820+1336_820+1337insGTGAAA NP_001138391.1:n.820+1336_820+1337insGTGAAA
NM_022970.3:c.1087+1336_1087+1337insGTGAAA NP_075259.4:n.1087+1336_1087+1337insGTGAAA
NM_023029.2:c.790_791insGTGAAA NP_075418.1:p.His264delinsArgGluAsn
NR_073009.1:n.1507_1508insGTGAAA
XM_006717708.2:c.1144+1336_1144+1337insGTGAAA XP_006717771.1:n.1144+1336_1144+1337insGTGAAA
XM_006717709.2:c.1114_1115insGTGAAA XP_006717772.1:p.His372delinsArgGluAsn
XM_006717710.2:c.1144+1336_1144+1337insGTGAAA XP_006717773.1:n.1144+1336_1144+1337insGTGAAA
XM_006717711.2:c.877+1336_877+1337insGTGAAA XP_006717774.1:n.877+1336_877+1337insGTGAAA
XM_006717712.2:c.799+1336_799+1337insGTGAAA XP_006717775.1:n.799+1336_799+1337insGTGAAA
XM_006717713.2:c.1114_1115insGTGAAA XP_006717776.1:p.His372delinsArgGluAsn
XM_011539510.1:c.373_374insGTGAAA XP_011537812.1:p.His125delinsArgGluAsn
NM_001320654.1:c.373_374insGTGAAA NP_001307583.1:p.His125delinsArgGluAsn
NM_001320658.1:c.1057_1058insGTGAAA NP_001307587.1:p.His353delinsArgGluAsn
XM_006717708.3:c.1144+1336_1144+1337insGTGAAA XP_006717771.1:n.1144+1336_1144+1337insGTGAAA
XM_006717710.4:c.1144+1336_1144+1337insGTGAAA XP_006717773.1:n.1144+1336_1144+1337insGTGAAA
XM_017015920.2:c.1144+1336_1144+1337insGTGAAA XP_016871409.1:n.1144+1336_1144+1337insGTGAAA
XM_017015921.2:c.1114_1115insGTGAAA XP_016871410.1:p.His372delinsArgGluAsn
XM_017015924.2:c.769_770insGTGAAA XP_016871413.1:p.His257delinsArgGluAsn
XM_017015925.2:c.769_770insGTGAAA XP_016871414.1:p.His257delinsArgGluAsn
XM_024447887.1:c.847_848insGTGAAA XP_024303655.1:p.His283delinsArgGluAsn
XM_024447888.1:c.877+1336_877+1337insGTGAAA XP_024303656.1:n.877+1336_877+1337insGTGAAA
XM_024447889.1:c.847_848insGTGAAA XP_024303657.1:p.His283delinsArgGluAsn
XM_024447890.1:c.877+1336_877+1337insGTGAAA XP_024303658.1:n.877+1336_877+1337insGTGAAA
XM_024447891.1:c.799+1336_799+1337insGTGAAA XP_024303659.1:n.799+1336_799+1337insGTGAAA
XM_024447892.1:c.-114_-113insGTGAAA XP_024303660.1:n.-114_-113insGTGAAA
NM_000141.5:c.1057_1058insGTGAAA MANE Select NP_000132.3:p.His353delinsArgGluAsn
NM_001144917.2:c.939+2633_939+2634insGTGAAA NP_001138389.1:n.939+2633_939+2634insGTGAAA
NM_001144918.2:c.712_713insGTGAAA NP_001138390.1:p.His238delinsArgGluAsn
NM_001144919.2:c.820+1336_820+1337insGTGAAA NP_001138391.1:n.820+1336_820+1337insGTGAAA
NM_001320658.2:c.1057_1058insGTGAAA NP_001307587.1:p.His353delinsArgGluAsn
NR_073009.2:n.1493_1494insGTGAAA
NM_001144915.2:c.790_791insGTGAAA NP_001138387.1:p.His264delinsArgGluAsn
NM_001144916.2:c.712_713insGTGAAA NP_001138388.1:p.His238delinsArgGluAsn
NM_001320654.2:c.373_374insGTGAAA NP_001307583.1:p.His125delinsArgGluAsn
Search 100 bp 5'
Search 100 bp 3'