Canonical Allele Identifier: CA1941016739
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121496546A= , CM000672.2:g.121496546A= GRCh38
NC_000010.10:g.123256060A= , CM000672.1:g.123256060A= GRCh37
NC_000010.9:g.123246050A= NCBI36
NG_012449.1:g.106913T=
NG_012449.2:g.106913T=

Transcript Alleles

HGVS Amino-acid Change
NM_000141.5:c.1849T= MANE Select NP_000132.3:p.Leu617=
ENST00000358487.10:c.1849T= MANE Select ENSP00000351276.6:p.Leu617=
ENST00000457416.7:c.1852T= MANE Plus Clinical ENSP00000410294.2:p.Leu618=
NM_000141.4:c.1849T= NP_000132.3:p.Leu617=
NM_001144913.1:c.1852T= NP_001138385.1:p.Leu618=
NM_001144914.1:c.1513T= NP_001138386.1:p.Leu505=
NM_001144915.1:c.1582T= NP_001138387.1:p.Leu528=
NM_001144915.2:c.1582T= NP_001138387.1:p.Leu528=
NM_001144916.1:c.1504T= NP_001138388.1:p.Leu502=
NM_001144916.2:c.1504T= NP_001138388.1:p.Leu502=
NM_001144917.1:c.1501T= NP_001138389.1:p.Leu501=
NM_001144917.2:c.1501T= NP_001138389.1:p.Leu501=
NM_001144918.1:c.1498T= NP_001138390.1:p.Leu500=
NM_001144918.2:c.1498T= NP_001138390.1:p.Leu500=
NM_001144919.1:c.1585T= NP_001138391.1:p.Leu529=
NM_001144919.2:c.1585T= NP_001138391.1:p.Leu529=
NM_001320654.1:c.1165T= NP_001307583.1:p.Leu389=
NM_001320654.2:c.1165T= NP_001307583.1:p.Leu389=
NM_001320658.1:c.1843T= NP_001307587.1:p.Leu615=
NM_001320658.2:c.1843T= NP_001307587.1:p.Leu615=
NM_022970.3:c.1852T= NP_075259.4:p.Leu618=
NM_023029.2:c.1582T= NP_075418.1:p.Leu528=
NR_073009.1:n.2299T=
NR_073009.2:n.2285T=
ENST00000336553.10:c.1576T= ENSP00000337665.6:p.Leu526=
ENST00000346997.6:c.1843T= ENSP00000263451.5:p.Leu615=
ENST00000351936.10:c.1849T= ENSP00000309878.9:p.Leu617=
ENST00000351936.11:c.1843T= ENSP00000309878.10:p.Leu615=
ENST00000356226.8:c.1498T= ENSP00000348559.4:p.Leu500=
ENST00000357555.9:c.1582T= ENSP00000350166.5:p.Leu528=
ENST00000358487.9:c.1849T= ENSP00000351276.5:p.Leu617=
ENST00000360144.7:c.1585T= ENSP00000353262.3:p.Leu529=
ENST00000369056.5:c.1852T= ENSP00000358052.1:p.Leu618=
ENST00000369058.7:c.1852T= ENSP00000358054.3:p.Leu618=
ENST00000369059.5:c.1507T= ENSP00000358055.1:p.Leu503=
ENST00000369060.8:c.1501T= ENSP00000358056.4:p.Leu501=
ENST00000369061.8:c.1513T= ENSP00000358057.4:p.Leu505=
ENST00000429361.5:c.625T= ENSP00000404219.1:p.Leu209=
ENST00000457416.6:c.1852T= ENSP00000410294.2:p.Leu618=
ENST00000478859.5:c.1165T= ENSP00000474011.1:p.Leu389=
ENST00000604236.5:c.*896T= ENSP00000474109.1:n.*896T=
ENST00000613048.4:c.1582T= ENSP00000484154.1:p.Leu528=
ENST00000638709.2:c.673T= ENSP00000491912.2:p.Leu225=
ENST00000682296.1:n.1191T=
ENST00000682550.1:c.1498T= ENSP00000507633.1:p.Leu500=
ENST00000682772.1:c.673T= ENSP00000506848.1:p.Leu225=
ENST00000682904.1:n.669T=
ENST00000683029.1:n.261T=
ENST00000683211.1:c.1843T= ENSP00000508257.1:p.Leu615=
ENST00000683250.1:c.*551T= ENSP00000506847.1:n.*551T=
ENST00000683418.1:n.4190T=
ENST00000684153.1:c.1498T= ENSP00000506937.1:p.Leu500=
ENST00000684516.1:n.2862T=
XM_006717708.2:c.1903T= XP_006717771.1:p.Leu635=
XM_006717708.3:c.1903T= XP_006717771.1:p.Leu635=
XM_006717709.2:c.1900T= XP_006717772.1:p.Leu634=
XM_006717710.2:c.1909T= XP_006717773.1:p.Leu637=
XM_006717710.4:c.1909T= XP_006717773.1:p.Leu637=
XM_006717711.2:c.1642T= XP_006717774.1:p.Leu548=
XM_006717712.2:c.1564T= XP_006717775.1:p.Leu522=
XM_006717713.2:c.1906T= XP_006717776.1:p.Leu636=
XM_011539510.1:c.1165T= XP_011537812.1:p.Leu389=
XM_017015920.2:c.1903T= XP_016871409.1:p.Leu635=
XM_017015921.2:c.1900T= XP_016871410.1:p.Leu634=
XM_017015924.2:c.1561T= XP_016871413.1:p.Leu521=
XM_017015925.2:c.1555T= XP_016871414.1:p.Leu519=
XM_024447887.1:c.1639T= XP_024303655.1:p.Leu547=
XM_024447888.1:c.1636T= XP_024303656.1:p.Leu546=
XM_024447889.1:c.1633T= XP_024303657.1:p.Leu545=
XM_024447890.1:c.1642T= XP_024303658.1:p.Leu548=
XM_024447891.1:c.1564T= XP_024303659.1:p.Leu522=
XM_024447892.1:c.679T= XP_024303660.1:p.Leu227=