Canonical Allele Identifier: CA365998110
Gene: TAB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.149379087C>A , CM000668.2:g.149379087C>A GRCh38
NC_000006.11:g.149700223C>A , CM000668.1:g.149700223C>A GRCh37
NC_000006.10:g.149741916C>A NCBI36
NG_021386.1:g.65788C>A
NG_021386.2:g.166164C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703212.1:n.1587C>A
ENST00000703213.1:c.1172C>A ENSP00000515239.1:p.Ala391Glu
ENST00000636456.1:c.320C>A ENSP00000490379.1:p.Ala107Glu
ENST00000637181.2:c.1172C>A MANE Select ENSP00000490618.1:p.Ala391Glu
ENST00000367456.5:c.1172C>A ENSP00000356426.1:p.Ala391Glu
ENST00000470466.5:c.1172C>A ENSP00000432709.1:p.Ala391Glu
ENST00000538427.5:c.1172C>A ENSP00000445752.1:p.Ala391Glu
NM_001292034.2:c.1172C>A NP_001278963.1:p.Ala391Glu
NM_001292035.2:c.1076C>A NP_001278964.1:p.Ala359Glu
NM_015093.5:c.1172C>A NP_055908.1:p.Ala391Glu
XM_006715403.2:c.1172C>A XP_006715466.1:p.Ala391Glu
XM_011535633.1:c.1172C>A XP_011533935.1:p.Ala391Glu
XM_011535634.1:c.1172C>A XP_011533936.1:p.Ala391Glu
XM_011535633.2:c.1172C>A XP_011533935.1:p.Ala391Glu
XM_017010591.1:c.1172C>A XP_016866080.1:p.Ala391Glu
XM_017010592.2:c.1172C>A XP_016866081.1:p.Ala391Glu
NM_001292034.3:c.1172C>A MANE Select NP_001278963.1:p.Ala391Glu
NM_001292035.3:c.1076C>A NP_001278964.1:p.Ala359Glu
NM_001369506.1:c.1172C>A NP_001356435.1:p.Ala391Glu
NM_015093.6:c.1172C>A NP_055908.1:p.Ala391Glu