Canonical Allele Identifier: CA16602761
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376315
dbSNP Id: rs1057519854

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488063A>T , CM000672.2:g.121488063A>T GRCh38
NC_000010.10:g.123247577A>T , CM000672.1:g.123247577A>T GRCh37
NC_000010.9:g.123237567A>T NCBI36
NG_012449.1:g.115396T>A
NG_012449.2:g.115396T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000457416.7:c.1917T>A MANE Plus Clinical ENSP00000410294.2:p.Asn639Lys
ENST00000351936.11:c.1908T>A ENSP00000309878.10:p.Asn636Lys
ENST00000638709.2:c.738T>A ENSP00000491912.2:p.Asn246Lys
ENST00000682296.1:n.1256T>A
ENST00000682550.1:c.1563T>A ENSP00000507633.1:p.Asn521Lys
ENST00000682772.1:c.738T>A ENSP00000506848.1:p.Asn246Lys
ENST00000682904.1:n.734T>A
ENST00000683029.1:n.326T>A
ENST00000683211.1:c.1908T>A ENSP00000508257.1:p.Asn636Lys
ENST00000683250.1:c.*616T>A ENSP00000506847.1:n.*616T>A
ENST00000683418.1:n.4255T>A
ENST00000684153.1:c.1563T>A ENSP00000506937.1:p.Asn521Lys
ENST00000684516.1:n.2927T>A
ENST00000358487.10:c.1914T>A MANE Select ENSP00000351276.6:p.Asn638Lys
ENST00000336553.10:c.1641T>A ENSP00000337665.6:p.Asn547Lys
ENST00000346997.6:c.1908T>A ENSP00000263451.5:p.Asn636Lys
ENST00000351936.10:c.1914T>A ENSP00000309878.9:p.Asn638Lys
ENST00000356226.8:c.1563T>A ENSP00000348559.4:p.Asn521Lys
ENST00000357555.9:c.1647T>A ENSP00000350166.5:p.Asn549Lys
ENST00000358487.9:c.1914T>A ENSP00000351276.5:p.Asn638Lys
ENST00000360144.7:c.1650T>A ENSP00000353262.3:p.Asn550Lys
ENST00000369056.5:c.1917T>A ENSP00000358052.1:p.Asn639Lys
ENST00000369058.7:c.1917T>A ENSP00000358054.3:p.Asn639Lys
ENST00000369059.5:c.1572T>A ENSP00000358055.1:p.Asn524Lys
ENST00000369060.8:c.1566T>A ENSP00000358056.4:p.Asn522Lys
ENST00000369061.8:c.1578T>A ENSP00000358057.4:p.Asn526Lys
ENST00000429361.5:c.690T>A ENSP00000404219.1:p.Asn230Lys
ENST00000457416.6:c.1917T>A ENSP00000410294.2:p.Asn639Lys
ENST00000478859.5:c.1230T>A ENSP00000474011.1:p.Asn410Lys
ENST00000604236.5:c.*961T>A ENSP00000474109.1:n.*961T>A
ENST00000613048.4:c.1647T>A ENSP00000484154.1:p.Asn549Lys
NM_000141.4:c.1914T>A NP_000132.3:p.Asn638Lys
NM_001144913.1:c.1917T>A NP_001138385.1:p.Asn639Lys
NM_001144914.1:c.1578T>A NP_001138386.1:p.Asn526Lys
NM_001144915.1:c.1647T>A NP_001138387.1:p.Asn549Lys
NM_001144916.1:c.1569T>A NP_001138388.1:p.Asn523Lys
NM_001144917.1:c.1566T>A NP_001138389.1:p.Asn522Lys
NM_001144918.1:c.1563T>A NP_001138390.1:p.Asn521Lys
NM_001144919.1:c.1650T>A NP_001138391.1:p.Asn550Lys
NM_022970.3:c.1917T>A NP_075259.4:p.Asn639Lys
NM_023029.2:c.1647T>A NP_075418.1:p.Asn549Lys
NR_073009.1:n.2364T>A
XM_006717708.2:c.1968T>A XP_006717771.1:p.Asn656Lys
XM_006717709.2:c.1965T>A XP_006717772.1:p.Asn655Lys
XM_006717710.2:c.1974T>A XP_006717773.1:p.Asn658Lys
XM_006717711.2:c.1707T>A XP_006717774.1:p.Asn569Lys
XM_006717712.2:c.1629T>A XP_006717775.1:p.Asn543Lys
XM_006717713.2:c.1971T>A XP_006717776.1:p.Asn657Lys
XM_011539510.1:c.1230T>A XP_011537812.1:p.Asn410Lys
NM_001320654.1:c.1230T>A NP_001307583.1:p.Asn410Lys
NM_001320658.1:c.1908T>A NP_001307587.1:p.Asn636Lys
XM_006717708.3:c.1968T>A XP_006717771.1:p.Asn656Lys
XM_006717710.4:c.1974T>A XP_006717773.1:p.Asn658Lys
XM_017015920.2:c.1968T>A XP_016871409.1:p.Asn656Lys
XM_017015921.2:c.1965T>A XP_016871410.1:p.Asn655Lys
XM_017015924.2:c.1626T>A XP_016871413.1:p.Asn542Lys
XM_017015925.2:c.1620T>A XP_016871414.1:p.Asn540Lys
XM_024447887.1:c.1704T>A XP_024303655.1:p.Asn568Lys
XM_024447888.1:c.1701T>A XP_024303656.1:p.Asn567Lys
XM_024447889.1:c.1698T>A XP_024303657.1:p.Asn566Lys
XM_024447890.1:c.1707T>A XP_024303658.1:p.Asn569Lys
XM_024447891.1:c.1629T>A XP_024303659.1:p.Asn543Lys
XM_024447892.1:c.744T>A XP_024303660.1:p.Asn248Lys
NM_000141.5:c.1914T>A MANE Select NP_000132.3:p.Asn638Lys
NM_001144917.2:c.1566T>A NP_001138389.1:p.Asn522Lys
NM_001144918.2:c.1563T>A NP_001138390.1:p.Asn521Lys
NM_001144919.2:c.1650T>A NP_001138391.1:p.Asn550Lys
NM_001320658.2:c.1908T>A NP_001307587.1:p.Asn636Lys
NR_073009.2:n.2350T>A
NM_001144915.2:c.1647T>A NP_001138387.1:p.Asn549Lys
NM_001144916.2:c.1569T>A NP_001138388.1:p.Asn523Lys
NM_001320654.2:c.1230T>A NP_001307583.1:p.Asn410Lys