Canonical Allele Identifier: CA378326992
Gene: FGFR2 HGNC NCBI

Linked Data

dbSNP Id: rs2134221007

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121515145T>G , CM000672.2:g.121515145T>G GRCh38
NC_000010.10:g.123274659T>G , CM000672.1:g.123274659T>G GRCh37
NC_000010.9:g.123264649T>G NCBI36
NG_012449.1:g.88314A>C
NG_012449.2:g.88314A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1262A>C MANE Plus Clinical ENSP00000410294.2:p.Lys421Thr
ENST00000351936.11:c.1259A>C ENSP00000309878.10:p.Lys420Thr
ENST00000638709.2:c.89A>C ENSP00000491912.2:p.Lys30Thr
ENST00000682296.1:n.607A>C
ENST00000682550.1:c.914A>C ENSP00000507633.1:p.Lys305Thr
ENST00000682772.1:c.89A>C ENSP00000506848.1:p.Lys30Thr
ENST00000683211.1:c.1259A>C ENSP00000508257.1:p.Lys420Thr
ENST00000683250.1:c.404-11204A>C ENSP00000506847.1:n.404-11204A>C
ENST00000683418.1:n.3606A>C
ENST00000684153.1:c.914A>C ENSP00000506937.1:p.Lys305Thr
ENST00000358487.10:c.1259A>C MANE Select ENSP00000351276.6:p.Lys420Thr
ENST00000336553.10:c.992A>C ENSP00000337665.6:p.Lys331Thr
ENST00000346997.6:c.1259A>C ENSP00000263451.5:p.Lys420Thr
ENST00000351936.10:c.1265A>C ENSP00000309878.9:p.Lys422Thr
ENST00000356226.8:c.914A>C ENSP00000348559.4:p.Lys305Thr
ENST00000357555.9:c.992A>C ENSP00000350166.5:p.Lys331Thr
ENST00000358487.9:c.1259A>C ENSP00000351276.5:p.Lys420Thr
ENST00000360144.7:c.995A>C ENSP00000353262.3:p.Lys332Thr
ENST00000369056.5:c.1262A>C ENSP00000358052.1:p.Lys421Thr
ENST00000369058.7:c.1262A>C ENSP00000358054.3:p.Lys421Thr
ENST00000369059.5:c.917A>C ENSP00000358055.1:p.Lys306Thr
ENST00000369060.8:c.939+4834A>C ENSP00000358056.4:n.939+4834A>C
ENST00000369061.8:c.923A>C ENSP00000358057.4:p.Lys308Thr
ENST00000429361.5:c.35A>C ENSP00000404219.1:p.Lys12Thr
ENST00000457416.6:c.1262A>C ENSP00000410294.2:p.Lys421Thr
ENST00000478859.5:c.575A>C ENSP00000474011.1:p.Lys192Thr
ENST00000604236.5:c.*306A>C ENSP00000474109.1:n.*306A>C
ENST00000613048.4:c.992A>C ENSP00000484154.1:p.Lys331Thr
NM_000141.4:c.1259A>C NP_000132.3:p.Lys420Thr
NM_001144913.1:c.1262A>C NP_001138385.1:p.Lys421Thr
NM_001144914.1:c.923A>C NP_001138386.1:p.Lys308Thr
NM_001144915.1:c.992A>C NP_001138387.1:p.Lys331Thr
NM_001144916.1:c.914A>C NP_001138388.1:p.Lys305Thr
NM_001144917.1:c.939+4834A>C NP_001138389.1:n.939+4834A>C
NM_001144918.1:c.914A>C NP_001138390.1:p.Lys305Thr
NM_001144919.1:c.995A>C NP_001138391.1:p.Lys332Thr
NM_022970.3:c.1262A>C NP_075259.4:p.Lys421Thr
NM_023029.2:c.992A>C NP_075418.1:p.Lys331Thr
NR_073009.1:n.1709A>C
XM_006717708.2:c.1319A>C XP_006717771.1:p.Lys440Thr
XM_006717709.2:c.1316A>C XP_006717772.1:p.Lys439Thr
XM_006717710.2:c.1319A>C XP_006717773.1:p.Lys440Thr
XM_006717711.2:c.1052A>C XP_006717774.1:p.Lys351Thr
XM_006717712.2:c.974A>C XP_006717775.1:p.Lys325Thr
XM_006717713.2:c.1316A>C XP_006717776.1:p.Lys439Thr
XM_011539510.1:c.575A>C XP_011537812.1:p.Lys192Thr
NM_001320654.1:c.575A>C NP_001307583.1:p.Lys192Thr
NM_001320658.1:c.1259A>C NP_001307587.1:p.Lys420Thr
XM_006717708.3:c.1319A>C XP_006717771.1:p.Lys440Thr
XM_006717710.4:c.1319A>C XP_006717773.1:p.Lys440Thr
XM_017015920.2:c.1319A>C XP_016871409.1:p.Lys440Thr
XM_017015921.2:c.1316A>C XP_016871410.1:p.Lys439Thr
XM_017015924.2:c.971A>C XP_016871413.1:p.Lys324Thr
XM_017015925.2:c.971A>C XP_016871414.1:p.Lys324Thr
XM_024447887.1:c.1049A>C XP_024303655.1:p.Lys350Thr
XM_024447888.1:c.1052A>C XP_024303656.1:p.Lys351Thr
XM_024447889.1:c.1049A>C XP_024303657.1:p.Lys350Thr
XM_024447890.1:c.1052A>C XP_024303658.1:p.Lys351Thr
XM_024447891.1:c.974A>C XP_024303659.1:p.Lys325Thr
XM_024447892.1:c.89A>C XP_024303660.1:p.Lys30Thr
NM_000141.5:c.1259A>C MANE Select NP_000132.3:p.Lys420Thr
NM_001144917.2:c.939+4834A>C NP_001138389.1:n.939+4834A>C
NM_001144918.2:c.914A>C NP_001138390.1:p.Lys305Thr
NM_001144919.2:c.995A>C NP_001138391.1:p.Lys332Thr
NM_001320658.2:c.1259A>C NP_001307587.1:p.Lys420Thr
NR_073009.2:n.1695A>C
NM_001144915.2:c.992A>C NP_001138387.1:p.Lys331Thr
NM_001144916.2:c.914A>C NP_001138388.1:p.Lys305Thr
NM_001320654.2:c.575A>C NP_001307583.1:p.Lys192Thr