Canonical Allele Identifier: CA1941012758
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121488052A= , CM000672.2:g.121488052A= GRCh38
NC_000010.10:g.123247566A= , CM000672.1:g.123247566A= GRCh37
NC_000010.9:g.123237556A= NCBI36
NG_012449.1:g.115407T=
NG_012449.2:g.115407T=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1925T= MANE Select NP_000132.3:p.Ile642=
ENST00000358487.10:c.1925T= MANE Select ENSP00000351276.6:p.Ile642=
ENST00000457416.7:c.1928T= MANE Plus Clinical ENSP00000410294.2:p.Ile643=
NM_000141.4:c.1925T= NP_000132.3:p.Ile642=
NM_001144913.1:c.1928T= NP_001138385.1:p.Ile643=
NM_001144914.1:c.1589T= NP_001138386.1:p.Ile530=
NM_001144915.1:c.1658T= NP_001138387.1:p.Ile553=
NM_001144915.2:c.1658T= NP_001138387.1:p.Ile553=
NM_001144916.1:c.1580T= NP_001138388.1:p.Ile527=
NM_001144916.2:c.1580T= NP_001138388.1:p.Ile527=
NM_001144917.1:c.1577T= NP_001138389.1:p.Ile526=
NM_001144917.2:c.1577T= NP_001138389.1:p.Ile526=
NM_001144918.1:c.1574T= NP_001138390.1:p.Ile525=
NM_001144918.2:c.1574T= NP_001138390.1:p.Ile525=
NM_001144919.1:c.1661T= NP_001138391.1:p.Ile554=
NM_001144919.2:c.1661T= NP_001138391.1:p.Ile554=
NM_001320654.1:c.1241T= NP_001307583.1:p.Ile414=
NM_001320654.2:c.1241T= NP_001307583.1:p.Ile414=
NM_001320658.1:c.1919T= NP_001307587.1:p.Ile640=
NM_001320658.2:c.1919T= NP_001307587.1:p.Ile640=
NM_022970.3:c.1928T= NP_075259.4:p.Ile643=
NM_023029.2:c.1658T= NP_075418.1:p.Ile553=
NR_073009.1:n.2375T=
NR_073009.2:n.2361T=
ENST00000336553.10:c.1652T= ENSP00000337665.6:p.Ile551=
ENST00000346997.6:c.1919T= ENSP00000263451.5:p.Ile640=
ENST00000351936.10:c.1925T= ENSP00000309878.9:p.Ile642=
ENST00000351936.11:c.1919T= ENSP00000309878.10:p.Ile640=
ENST00000356226.8:c.1574T= ENSP00000348559.4:p.Ile525=
ENST00000357555.9:c.1658T= ENSP00000350166.5:p.Ile553=
ENST00000358487.9:c.1925T= ENSP00000351276.5:p.Ile642=
ENST00000360144.7:c.1661T= ENSP00000353262.3:p.Ile554=
ENST00000369056.5:c.1928T= ENSP00000358052.1:p.Ile643=
ENST00000369058.7:c.1928T= ENSP00000358054.3:p.Ile643=
ENST00000369059.5:c.1583T= ENSP00000358055.1:p.Ile528=
ENST00000369060.8:c.1577T= ENSP00000358056.4:p.Ile526=
ENST00000369061.8:c.1589T= ENSP00000358057.4:p.Ile530=
ENST00000429361.5:c.701T= ENSP00000404219.1:p.Ile234=
ENST00000457416.6:c.1928T= ENSP00000410294.2:p.Ile643=
ENST00000478859.5:c.1241T= ENSP00000474011.1:p.Ile414=
ENST00000604236.5:c.*972T= ENSP00000474109.1:n.*972T=
ENST00000613048.4:c.1658T= ENSP00000484154.1:p.Ile553=
ENST00000638709.2:c.749T= ENSP00000491912.2:p.Ile250=
ENST00000682296.1:n.1267T=
ENST00000682550.1:c.1574T= ENSP00000507633.1:p.Ile525=
ENST00000682772.1:c.749T= ENSP00000506848.1:p.Ile250=
ENST00000682904.1:n.745T=
ENST00000683029.1:n.337T=
ENST00000683211.1:c.1919T= ENSP00000508257.1:p.Ile640=
ENST00000683250.1:c.*627T= ENSP00000506847.1:n.*627T=
ENST00000683418.1:n.4266T=
ENST00000684153.1:c.1574T= ENSP00000506937.1:p.Ile525=
ENST00000684516.1:n.2938T=
XM_006717708.2:c.1979T= XP_006717771.1:p.Ile660=
XM_006717708.3:c.1979T= XP_006717771.1:p.Ile660=
XM_006717709.2:c.1976T= XP_006717772.1:p.Ile659=
XM_006717710.2:c.1985T= XP_006717773.1:p.Ile662=
XM_006717710.4:c.1985T= XP_006717773.1:p.Ile662=
XM_006717711.2:c.1718T= XP_006717774.1:p.Ile573=
XM_006717712.2:c.1640T= XP_006717775.1:p.Ile547=
XM_006717713.2:c.1982T= XP_006717776.1:p.Ile661=
XM_011539510.1:c.1241T= XP_011537812.1:p.Ile414=
XM_017015920.2:c.1979T= XP_016871409.1:p.Ile660=
XM_017015921.2:c.1976T= XP_016871410.1:p.Ile659=
XM_017015924.2:c.1637T= XP_016871413.1:p.Ile546=
XM_017015925.2:c.1631T= XP_016871414.1:p.Ile544=
XM_024447887.1:c.1715T= XP_024303655.1:p.Ile572=
XM_024447888.1:c.1712T= XP_024303656.1:p.Ile571=
XM_024447889.1:c.1709T= XP_024303657.1:p.Ile570=
XM_024447890.1:c.1718T= XP_024303658.1:p.Ile573=
XM_024447891.1:c.1640T= XP_024303659.1:p.Ile547=
XM_024447892.1:c.755T= XP_024303660.1:p.Ile252=