Canonical Allele Identifier: CA1941012683
Gene: FGFR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.121487857A= , CM000672.2:g.121487857A= GRCh38
NC_000010.10:g.123247371A= , CM000672.1:g.123247371A= GRCh37
NC_000010.9:g.123237361A= NCBI36
NG_012449.1:g.115602T=
NG_012449.2:g.115602T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000457416.7:c.1989+134T= MANE Plus Clinical ENSP00000410294.2:n.1989+134T=
ENST00000351936.11:c.1980+134T= ENSP00000309878.10:n.1980+134T=
ENST00000638709.2:c.810+134T= ENSP00000491912.2:n.810+134T=
ENST00000682296.1:n.1328+134T=
ENST00000682550.1:c.1635+134T= ENSP00000507633.1:n.1635+134T=
ENST00000682772.1:c.810+134T= ENSP00000506848.1:n.810+134T=
ENST00000682904.1:n.806+134T=
ENST00000683029.1:n.398+134T=
ENST00000683211.1:c.1980+134T= ENSP00000508257.1:n.1980+134T=
ENST00000683250.1:c.*688+134T= ENSP00000506847.1:n.*688+134T=
ENST00000683418.1:n.4327+134T=
ENST00000684153.1:c.1635+134T= ENSP00000506937.1:n.1635+134T=
ENST00000684516.1:n.2999+134T=
ENST00000358487.10:c.1986+134T= MANE Select ENSP00000351276.6:n.1986+134T=
ENST00000336553.10:c.1713+134T= ENSP00000337665.6:n.1713+134T=
ENST00000346997.6:c.1980+134T= ENSP00000263451.5:n.1980+134T=
ENST00000351936.10:c.1986+134T= ENSP00000309878.9:n.1986+134T=
ENST00000356226.8:c.1635+134T= ENSP00000348559.4:n.1635+134T=
ENST00000357555.9:c.1719+134T= ENSP00000350166.5:n.1719+134T=
ENST00000358487.9:c.1986+134T= ENSP00000351276.5:n.1986+134T=
ENST00000360144.7:c.1722+134T= ENSP00000353262.3:n.1722+134T=
ENST00000369056.5:c.1989+134T= ENSP00000358052.1:n.1989+134T=
ENST00000369058.7:c.1989+134T= ENSP00000358054.3:n.1989+134T=
ENST00000369059.5:c.1644+134T= ENSP00000358055.1:n.1644+134T=
ENST00000369060.8:c.1638+134T= ENSP00000358056.4:n.1638+134T=
ENST00000369061.8:c.1650+134T= ENSP00000358057.4:n.1650+134T=
ENST00000429361.5:c.762+134T= ENSP00000404219.1:n.762+134T=
ENST00000457416.6:c.1989+134T= ENSP00000410294.2:n.1989+134T=
ENST00000478859.5:c.1302+134T= ENSP00000474011.1:n.1302+134T=
ENST00000604236.5:c.*1033+134T= ENSP00000474109.1:n.*1033+134T=
ENST00000613048.4:c.1719+134T= ENSP00000484154.1:n.1719+134T=
NM_000141.4:c.1986+134T= NP_000132.3:n.1986+134T=
NM_001144913.1:c.1989+134T= NP_001138385.1:n.1989+134T=
NM_001144914.1:c.1650+134T= NP_001138386.1:n.1650+134T=
NM_001144915.1:c.1719+134T= NP_001138387.1:n.1719+134T=
NM_001144916.1:c.1641+134T= NP_001138388.1:n.1641+134T=
NM_001144917.1:c.1638+134T= NP_001138389.1:n.1638+134T=
NM_001144918.1:c.1635+134T= NP_001138390.1:n.1635+134T=
NM_001144919.1:c.1722+134T= NP_001138391.1:n.1722+134T=
NM_022970.3:c.1989+134T= NP_075259.4:n.1989+134T=
NM_023029.2:c.1719+134T= NP_075418.1:n.1719+134T=
NR_073009.1:n.2436+134T=
XM_006717708.2:c.2040+134T= XP_006717771.1:n.2040+134T=
XM_006717709.2:c.2037+134T= XP_006717772.1:n.2037+134T=
XM_006717710.2:c.2046+134T= XP_006717773.1:n.2046+134T=
XM_006717711.2:c.1779+134T= XP_006717774.1:n.1779+134T=
XM_006717712.2:c.1701+134T= XP_006717775.1:n.1701+134T=
XM_006717713.2:c.2043+134T= XP_006717776.1:n.2043+134T=
XM_011539510.1:c.1302+134T= XP_011537812.1:n.1302+134T=
NM_001320654.1:c.1302+134T= NP_001307583.1:n.1302+134T=
NM_001320658.1:c.1980+134T= NP_001307587.1:n.1980+134T=
XM_006717708.3:c.2040+134T= XP_006717771.1:n.2040+134T=
XM_006717710.4:c.2046+134T= XP_006717773.1:n.2046+134T=
XM_017015920.2:c.2040+134T= XP_016871409.1:n.2040+134T=
XM_017015921.2:c.2037+134T= XP_016871410.1:n.2037+134T=
XM_017015924.2:c.1698+134T= XP_016871413.1:n.1698+134T=
XM_017015925.2:c.1692+134T= XP_016871414.1:n.1692+134T=
XM_024447887.1:c.1776+134T= XP_024303655.1:n.1776+134T=
XM_024447888.1:c.1773+134T= XP_024303656.1:n.1773+134T=
XM_024447889.1:c.1770+134T= XP_024303657.1:n.1770+134T=
XM_024447890.1:c.1779+134T= XP_024303658.1:n.1779+134T=
XM_024447891.1:c.1701+134T= XP_024303659.1:n.1701+134T=
XM_024447892.1:c.816+134T= XP_024303660.1:n.816+134T=
NM_000141.5:c.1986+134T= MANE Select NP_000132.3:n.1986+134T=
NM_001144917.2:c.1638+134T= NP_001138389.1:n.1638+134T=
NM_001144918.2:c.1635+134T= NP_001138390.1:n.1635+134T=
NM_001144919.2:c.1722+134T= NP_001138391.1:n.1722+134T=
NM_001320658.2:c.1980+134T= NP_001307587.1:n.1980+134T=
NR_073009.2:n.2422+134T=
NM_001144915.2:c.1719+134T= NP_001138387.1:n.1719+134T=
NM_001144916.2:c.1641+134T= NP_001138388.1:n.1641+134T=
NM_001320654.2:c.1302+134T= NP_001307583.1:n.1302+134T=