Canonical Allele Identifier: CA280180
Gene: FGFR2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13279
ClinVar RCV Id: RCV000014201
dbSNP Id: rs121918498

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121520162_121520163delinsAA , CM000672.2:g.121520162_121520163delinsAA GRCh38
NC_000010.10:g.123279676_123279677delinsAA , CM000672.1:g.123279676_123279677delinsAA GRCh37
NC_000010.9:g.123269666_123269667delinsAA NCBI36
NG_012449.1:g.83296_83297delinsTT
NG_012449.2:g.83296_83297delinsTT

Transcript Alleles

HGVS Amino-acid change
NM_000141.4:c.755_756delinsTT VV NP_000132.3:p.Ser252Phe
NM_001144913.1:c.755_756delinsTT VV NP_001138385.1:p.Ser252Phe
NM_001144914.1:c.749-4844_749-4843delinsTT VV NP_001138386.1:p.=
NM_001144915.1:c.488_489delinsTT VV NP_001138387.1:p.Ser163Phe
NM_001144916.1:c.410_411delinsTT VV NP_001138388.1:p.Ser137Phe
NM_001144917.1:c.755_756delinsTT VV NP_001138389.1:p.Ser252Phe
NM_001144918.1:c.410_411delinsTT VV NP_001138390.1:p.Ser137Phe
NM_001144919.1:c.488_489delinsTT VV NP_001138391.1:p.Ser163Phe
NM_022970.3:c.755_756delinsTT VV NP_075259.4:p.Ser252Phe
NM_023029.2:c.488_489delinsTT VV NP_075418.1:p.Ser163Phe
NR_073009.1:n.1057_1058delinsTT
XM_006717708.2:c.812_813delinsTT XP_006717771.1:p.Ser271Phe
XM_006717709.2:c.812_813delinsTT XP_006717772.1:p.Ser271Phe
XM_006717710.2:c.812_813delinsTT XP_006717773.1:p.Ser271Phe
XM_006717711.2:c.545_546delinsTT XP_006717774.1:p.Ser182Phe
XM_006717712.2:c.467_468delinsTT XP_006717775.1:p.Ser156Phe
XM_006717713.2:c.812_813delinsTT XP_006717776.1:p.Ser271Phe
XM_011539510.1:c.71_72delinsTT XP_011537812.1:p.Ser24Phe
NM_001320654.1:c.71_72delinsTT VV NP_001307583.1:p.Ser24Phe
NM_001320658.1:c.755_756delinsTT VV NP_001307587.1:p.Ser252Phe
XM_006717708.3:c.812_813delinsTT XP_006717771.1:p.Ser271Phe
XM_006717710.4:c.812_813delinsTT XP_006717773.1:p.Ser271Phe
XM_017015920.2:c.812_813delinsTT XP_016871409.1:p.Ser271Phe
XM_017015921.2:c.812_813delinsTT XP_016871410.1:p.Ser271Phe
XM_017015924.2:c.467_468delinsTT XP_016871413.1:p.Ser156Phe
XM_017015925.2:c.467_468delinsTT XP_016871414.1:p.Ser156Phe
XM_024447887.1:c.545_546delinsTT XP_024303655.1:p.Ser182Phe
XM_024447888.1:c.545_546delinsTT XP_024303656.1:p.Ser182Phe
XM_024447889.1:c.545_546delinsTT XP_024303657.1:p.Ser182Phe
XM_024447890.1:c.545_546delinsTT XP_024303658.1:p.Ser182Phe
XM_024447891.1:c.467_468delinsTT XP_024303659.1:p.Ser156Phe
XM_024447892.1:c.-416_-415delinsTT XP_024303660.1:p.=
ENST00000336553.10:c.488_489delinsTT ENSP00000337665.6:p.Ser163Phe
ENST00000346997.6:c.755_756delinsTT ENSP00000263451.5:p.Ser252Phe
ENST00000351936.10:c.755_756delinsTT ENSP00000309878.9:p.Ser252Phe
ENST00000356226.8:c.410_411delinsTT ENSP00000348559.4:p.Ser137Phe
ENST00000357555.9:c.488_489delinsTT ENSP00000350166.5:p.Ser163Phe
ENST00000358487.9:c.755_756delinsTT ENSP00000351276.5:p.Ser252Phe
ENST00000360144.7:c.488_489delinsTT ENSP00000353262.3:p.Ser163Phe
ENST00000369056.5:c.755_756delinsTT ENSP00000358052.1:p.Ser252Phe
ENST00000369058.7:c.755_756delinsTT ENSP00000358054.3:p.Ser252Phe
ENST00000369059.5:c.410_411delinsTT ENSP00000358055.1:p.Ser137Phe
ENST00000369060.8:c.755_756delinsTT ENSP00000358056.4:p.Ser252Phe
ENST00000369061.8:c.749-4844_749-4843delinsTT ENSP00000358057.4:p.=
ENST00000457416.6:c.755_756delinsTT ENSP00000410294.2:p.Ser252Phe
ENST00000478859.5:c.71_72delinsTT ENSP00000474011.1:p.Ser24Phe
ENST00000490349.5:n.1016_1017delinsTT
ENST00000604236.5:c.410_411delinsTT ENSP00000474109.1:p.Ser137Phe
ENST00000613048.4:c.488_489delinsTT ENSP00000484154.1:p.Ser163Phe