Canonical Allele Identifier: CA16043907
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121498521_121498522delinsAG , CM000672.2:g.121498521_121498522delinsAG GRCh38
NC_000010.10:g.123258035_123258036delinsAG , CM000672.1:g.123258035_123258036delinsAG GRCh37
NC_000010.9:g.123248025_123248026delinsAG NCBI36
NG_012449.1:g.104937_104938delinsCT
NG_012449.2:g.104937_104938delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1648_1649delinsCT MANE Plus Clinical ENSP00000410294.2:p.Asn550Leu
ENST00000351936.11:c.1639_1640delinsCT ENSP00000309878.10:p.Asn547Leu
ENST00000638709.2:c.469_470delinsCT ENSP00000491912.2:p.Asn157Leu
ENST00000682296.1:n.987_988delinsCT
ENST00000682550.1:c.1294_1295delinsCT ENSP00000507633.1:p.Asn432Leu
ENST00000682772.1:c.469_470delinsCT ENSP00000506848.1:p.Asn157Leu
ENST00000682904.1:n.465_466delinsCT
ENST00000683211.1:c.1639_1640delinsCT ENSP00000508257.1:p.Asn547Leu
ENST00000683250.1:c.*347_*348delinsCT ENSP00000506847.1:n.*347_*348delinsCT
ENST00000683418.1:n.3986_3987delinsCT
ENST00000684153.1:c.1294_1295delinsCT ENSP00000506937.1:p.Asn432Leu
ENST00000684516.1:n.2658_2659delinsCT
ENST00000358487.10:c.1645_1646delinsCT MANE Select ENSP00000351276.6:p.Asn549Leu
ENST00000336553.10:c.1372_1373delinsCT ENSP00000337665.6:p.Asn458Leu
ENST00000346997.6:c.1639_1640delinsCT ENSP00000263451.5:p.Asn547Leu
ENST00000351936.10:c.1645_1646delinsCT ENSP00000309878.9:p.Asn549Leu
ENST00000356226.8:c.1294_1295delinsCT ENSP00000348559.4:p.Asn432Leu
ENST00000357555.9:c.1378_1379delinsCT ENSP00000350166.5:p.Asn460Leu
ENST00000358487.9:c.1645_1646delinsCT ENSP00000351276.5:p.Asn549Leu
ENST00000360144.7:c.1381_1382delinsCT ENSP00000353262.3:p.Asn461Leu
ENST00000369056.5:c.1648_1649delinsCT ENSP00000358052.1:p.Asn550Leu
ENST00000369058.7:c.1648_1649delinsCT ENSP00000358054.3:p.Asn550Leu
ENST00000369059.5:c.1303_1304delinsCT ENSP00000358055.1:p.Asn435Leu
ENST00000369060.8:c.1297_1298delinsCT ENSP00000358056.4:p.Asn433Leu
ENST00000369061.8:c.1309_1310delinsCT ENSP00000358057.4:p.Asn437Leu
ENST00000429361.5:c.421_422delinsCT ENSP00000404219.1:p.Asn141Leu
ENST00000457416.6:c.1648_1649delinsCT ENSP00000410294.2:p.Asn550Leu
ENST00000478859.5:c.961_962delinsCT ENSP00000474011.1:p.Asn321Leu
ENST00000604236.5:c.*692_*693delinsCT ENSP00000474109.1:n.*692_*693delinsCT
ENST00000613048.4:c.1378_1379delinsCT ENSP00000484154.1:p.Asn460Leu
NM_000141.4:c.1645_1646delinsCT NP_000132.3:p.Asn549Leu
NM_001144913.1:c.1648_1649delinsCT NP_001138385.1:p.Asn550Leu
NM_001144914.1:c.1309_1310delinsCT NP_001138386.1:p.Asn437Leu
NM_001144915.1:c.1378_1379delinsCT NP_001138387.1:p.Asn460Leu
NM_001144916.1:c.1300_1301delinsCT NP_001138388.1:p.Asn434Leu
NM_001144917.1:c.1297_1298delinsCT NP_001138389.1:p.Asn433Leu
NM_001144918.1:c.1294_1295delinsCT NP_001138390.1:p.Asn432Leu
NM_001144919.1:c.1381_1382delinsCT NP_001138391.1:p.Asn461Leu
NM_022970.3:c.1648_1649delinsCT NP_075259.4:p.Asn550Leu
NM_023029.2:c.1378_1379delinsCT NP_075418.1:p.Asn460Leu
NR_073009.1:n.2095_2096delinsCT
XM_006717708.2:c.1699_1700delinsCT XP_006717771.1:p.Asn567Leu
XM_006717709.2:c.1696_1697delinsCT XP_006717772.1:p.Asn566Leu
XM_006717710.2:c.1705_1706delinsCT XP_006717773.1:p.Asn569Leu
XM_006717711.2:c.1438_1439delinsCT XP_006717774.1:p.Asn480Leu
XM_006717712.2:c.1360_1361delinsCT XP_006717775.1:p.Asn454Leu
XM_006717713.2:c.1702_1703delinsCT XP_006717776.1:p.Asn568Leu
XM_011539510.1:c.961_962delinsCT XP_011537812.1:p.Asn321Leu
NM_001320654.1:c.961_962delinsCT NP_001307583.1:p.Asn321Leu
NM_001320658.1:c.1639_1640delinsCT NP_001307587.1:p.Asn547Leu
XM_006717708.3:c.1699_1700delinsCT XP_006717771.1:p.Asn567Leu
XM_006717710.4:c.1705_1706delinsCT XP_006717773.1:p.Asn569Leu
XM_017015920.2:c.1699_1700delinsCT XP_016871409.1:p.Asn567Leu
XM_017015921.2:c.1696_1697delinsCT XP_016871410.1:p.Asn566Leu
XM_017015924.2:c.1357_1358delinsCT XP_016871413.1:p.Asn453Leu
XM_017015925.2:c.1351_1352delinsCT XP_016871414.1:p.Asn451Leu
XM_024447887.1:c.1435_1436delinsCT XP_024303655.1:p.Asn479Leu
XM_024447888.1:c.1432_1433delinsCT XP_024303656.1:p.Asn478Leu
XM_024447889.1:c.1429_1430delinsCT XP_024303657.1:p.Asn477Leu
XM_024447890.1:c.1438_1439delinsCT XP_024303658.1:p.Asn480Leu
XM_024447891.1:c.1360_1361delinsCT XP_024303659.1:p.Asn454Leu
XM_024447892.1:c.475_476delinsCT XP_024303660.1:p.Asn159Leu
NM_000141.5:c.1645_1646delinsCT MANE Select NP_000132.3:p.Asn549Leu
NM_001144917.2:c.1297_1298delinsCT NP_001138389.1:p.Asn433Leu
NM_001144918.2:c.1294_1295delinsCT NP_001138390.1:p.Asn432Leu
NM_001144919.2:c.1381_1382delinsCT NP_001138391.1:p.Asn461Leu
NM_001320658.2:c.1639_1640delinsCT NP_001307587.1:p.Asn547Leu
NR_073009.2:n.2081_2082delinsCT
NM_001144915.2:c.1378_1379delinsCT NP_001138387.1:p.Asn460Leu
NM_001144916.2:c.1300_1301delinsCT NP_001138388.1:p.Asn434Leu
NM_001320654.2:c.961_962delinsCT NP_001307583.1:p.Asn321Leu