Canonical Allele Identifier: CA2580082426
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2063949
ClinVar RCV Id: RCV002943092

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498613_121498614delinsTT , CM000672.2:g.121498613_121498614delinsTT GRCh38
NC_000010.10:g.123258127_123258128delinsTT , CM000672.1:g.123258127_123258128delinsTT GRCh37
NC_000010.9:g.123248117_123248118delinsTT NCBI36
NG_012449.1:g.104845_104846delinsAA
NG_012449.2:g.104845_104846delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1565-9_1565-8delinsAA MANE Plus Clinical ENSP00000410294.2:n.1565-9_1565-8delinsAA
ENST00000351936.11:c.1556-9_1556-8delinsAA ENSP00000309878.10:n.1556-9_1556-8delinsAA
ENST00000638709.2:c.386-9_386-8delinsAA ENSP00000491912.2:n.386-9_386-8delinsAA
ENST00000682296.1:n.904-9_904-8delinsAA
ENST00000682550.1:c.1211-9_1211-8delinsAA ENSP00000507633.1:n.1211-9_1211-8delinsAA
ENST00000682772.1:c.386-9_386-8delinsAA ENSP00000506848.1:n.386-9_386-8delinsAA
ENST00000682904.1:n.382-9_382-8delinsAA
ENST00000683211.1:c.1556-9_1556-8delinsAA ENSP00000508257.1:n.1556-9_1556-8delinsAA
ENST00000683250.1:c.*264-9_*264-8delinsAA ENSP00000506847.1:n.*264-9_*264-8delinsAA
ENST00000683418.1:n.3903-9_3903-8delinsAA
ENST00000684153.1:c.1211-9_1211-8delinsAA ENSP00000506937.1:n.1211-9_1211-8delinsAA
ENST00000684516.1:n.2575-9_2575-8delinsAA
ENST00000358487.10:c.1562-9_1562-8delinsAA MANE Select ENSP00000351276.6:n.1562-9_1562-8delinsAA
ENST00000336553.10:c.1289-9_1289-8delinsAA ENSP00000337665.6:n.1289-9_1289-8delinsAA
ENST00000346997.6:c.1556-9_1556-8delinsAA ENSP00000263451.5:n.1556-9_1556-8delinsAA
ENST00000351936.10:c.1562-9_1562-8delinsAA ENSP00000309878.9:n.1562-9_1562-8delinsAA
ENST00000356226.8:c.1211-9_1211-8delinsAA ENSP00000348559.4:n.1211-9_1211-8delinsAA
ENST00000357555.9:c.1295-9_1295-8delinsAA ENSP00000350166.5:n.1295-9_1295-8delinsAA
ENST00000358487.9:c.1562-9_1562-8delinsAA ENSP00000351276.5:n.1562-9_1562-8delinsAA
ENST00000360144.7:c.1298-9_1298-8delinsAA ENSP00000353262.3:n.1298-9_1298-8delinsAA
ENST00000369056.5:c.1565-9_1565-8delinsAA ENSP00000358052.1:n.1565-9_1565-8delinsAA
ENST00000369058.7:c.1565-9_1565-8delinsAA ENSP00000358054.3:n.1565-9_1565-8delinsAA
ENST00000369059.5:c.1220-9_1220-8delinsAA ENSP00000358055.1:n.1220-9_1220-8delinsAA
ENST00000369060.8:c.1214-9_1214-8delinsAA ENSP00000358056.4:n.1214-9_1214-8delinsAA
ENST00000369061.8:c.1226-9_1226-8delinsAA ENSP00000358057.4:n.1226-9_1226-8delinsAA
ENST00000429361.5:c.338-9_338-8delinsAA ENSP00000404219.1:n.338-9_338-8delinsAA
ENST00000457416.6:c.1565-9_1565-8delinsAA ENSP00000410294.2:n.1565-9_1565-8delinsAA
ENST00000478859.5:c.878-9_878-8delinsAA ENSP00000474011.1:n.878-9_878-8delinsAA
ENST00000604236.5:c.*609-9_*609-8delinsAA ENSP00000474109.1:n.*609-9_*609-8delinsAA
ENST00000613048.4:c.1295-9_1295-8delinsAA ENSP00000484154.1:n.1295-9_1295-8delinsAA
NM_000141.4:c.1562-9_1562-8delinsAA NP_000132.3:n.1562-9_1562-8delinsAA
NM_001144913.1:c.1565-9_1565-8delinsAA NP_001138385.1:n.1565-9_1565-8delinsAA
NM_001144914.1:c.1226-9_1226-8delinsAA NP_001138386.1:n.1226-9_1226-8delinsAA
NM_001144915.1:c.1295-9_1295-8delinsAA NP_001138387.1:n.1295-9_1295-8delinsAA
NM_001144916.1:c.1217-9_1217-8delinsAA NP_001138388.1:n.1217-9_1217-8delinsAA
NM_001144917.1:c.1214-9_1214-8delinsAA NP_001138389.1:n.1214-9_1214-8delinsAA
NM_001144918.1:c.1211-9_1211-8delinsAA NP_001138390.1:n.1211-9_1211-8delinsAA
NM_001144919.1:c.1298-9_1298-8delinsAA NP_001138391.1:n.1298-9_1298-8delinsAA
NM_022970.3:c.1565-9_1565-8delinsAA NP_075259.4:n.1565-9_1565-8delinsAA
NM_023029.2:c.1295-9_1295-8delinsAA NP_075418.1:n.1295-9_1295-8delinsAA
NR_073009.1:n.2012-9_2012-8delinsAA
XM_006717708.2:c.1616-9_1616-8delinsAA XP_006717771.1:n.1616-9_1616-8delinsAA
XM_006717709.2:c.1613-9_1613-8delinsAA XP_006717772.1:n.1613-9_1613-8delinsAA
XM_006717710.2:c.1622-9_1622-8delinsAA XP_006717773.1:n.1622-9_1622-8delinsAA
XM_006717711.2:c.1355-9_1355-8delinsAA XP_006717774.1:n.1355-9_1355-8delinsAA
XM_006717712.2:c.1277-9_1277-8delinsAA XP_006717775.1:n.1277-9_1277-8delinsAA
XM_006717713.2:c.1619-9_1619-8delinsAA XP_006717776.1:n.1619-9_1619-8delinsAA
XM_011539510.1:c.878-9_878-8delinsAA XP_011537812.1:n.878-9_878-8delinsAA
NM_001320654.1:c.878-9_878-8delinsAA NP_001307583.1:n.878-9_878-8delinsAA
NM_001320658.1:c.1556-9_1556-8delinsAA NP_001307587.1:n.1556-9_1556-8delinsAA
XM_006717708.3:c.1616-9_1616-8delinsAA XP_006717771.1:n.1616-9_1616-8delinsAA
XM_006717710.4:c.1622-9_1622-8delinsAA XP_006717773.1:n.1622-9_1622-8delinsAA
XM_017015920.2:c.1616-9_1616-8delinsAA XP_016871409.1:n.1616-9_1616-8delinsAA
XM_017015921.2:c.1613-9_1613-8delinsAA XP_016871410.1:n.1613-9_1613-8delinsAA
XM_017015924.2:c.1274-9_1274-8delinsAA XP_016871413.1:n.1274-9_1274-8delinsAA
XM_017015925.2:c.1268-9_1268-8delinsAA XP_016871414.1:n.1268-9_1268-8delinsAA
XM_024447887.1:c.1352-9_1352-8delinsAA XP_024303655.1:n.1352-9_1352-8delinsAA
XM_024447888.1:c.1349-9_1349-8delinsAA XP_024303656.1:n.1349-9_1349-8delinsAA
XM_024447889.1:c.1346-9_1346-8delinsAA XP_024303657.1:n.1346-9_1346-8delinsAA
XM_024447890.1:c.1355-9_1355-8delinsAA XP_024303658.1:n.1355-9_1355-8delinsAA
XM_024447891.1:c.1277-9_1277-8delinsAA XP_024303659.1:n.1277-9_1277-8delinsAA
XM_024447892.1:c.392-9_392-8delinsAA XP_024303660.1:n.392-9_392-8delinsAA
NM_000141.5:c.1562-9_1562-8delinsAA MANE Select NP_000132.3:n.1562-9_1562-8delinsAA
NM_001144917.2:c.1214-9_1214-8delinsAA NP_001138389.1:n.1214-9_1214-8delinsAA
NM_001144918.2:c.1211-9_1211-8delinsAA NP_001138390.1:n.1211-9_1211-8delinsAA
NM_001144919.2:c.1298-9_1298-8delinsAA NP_001138391.1:n.1298-9_1298-8delinsAA
NM_001320658.2:c.1556-9_1556-8delinsAA NP_001307587.1:n.1556-9_1556-8delinsAA
NR_073009.2:n.1998-9_1998-8delinsAA
NM_001144915.2:c.1295-9_1295-8delinsAA NP_001138387.1:n.1295-9_1295-8delinsAA
NM_001144916.2:c.1217-9_1217-8delinsAA NP_001138388.1:n.1217-9_1217-8delinsAA
NM_001320654.2:c.878-9_878-8delinsAA NP_001307583.1:n.878-9_878-8delinsAA