Canonical Allele Identifier: CA365996261

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378537C>A , CM000668.2:g.149378537C>A	GRCh38
NC_000006.11:g.149699673C>A , CM000668.1:g.149699673C>A	GRCh37
NC_000006.10:g.149741366C>A	NCBI36
NG_021386.1:g.65238C>A
NG_021386.2:g.165614C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001292034.3:c.622C>A MANE Select	NP_001278963.1:p.Pro208Thr
ENST00000637181.2:c.622C>A MANE Select	ENSP00000490618.1:p.Pro208Thr
NM_001292034.2:c.622C>A	NP_001278963.1:p.Pro208Thr
NM_001292035.2:c.526C>A	NP_001278964.1:p.Pro176Thr
NM_001292035.3:c.526C>A	NP_001278964.1:p.Pro176Thr
NM_001369506.1:c.622C>A	NP_001356435.1:p.Pro208Thr
NM_015093.5:c.622C>A	NP_055908.1:p.Pro208Thr
NM_015093.6:c.622C>A	NP_055908.1:p.Pro208Thr
ENST00000367456.5:c.622C>A	ENSP00000356426.1:p.Pro208Thr
ENST00000470466.5:c.622C>A	ENSP00000432709.1:p.Pro208Thr
ENST00000538427.5:c.622C>A	ENSP00000445752.1:p.Pro208Thr
ENST00000636456.1:c.-96-135C>A	ENSP00000490379.1:n.-96-135C>A
ENST00000703212.1:n.1037C>A
ENST00000703213.1:c.622C>A	ENSP00000515239.1:p.Pro208Thr
XM_006715403.2:c.622C>A	XP_006715466.1:p.Pro208Thr
XM_011535633.1:c.622C>A	XP_011533935.1:p.Pro208Thr
XM_011535633.2:c.622C>A	XP_011533935.1:p.Pro208Thr
XM_011535634.1:c.622C>A	XP_011533936.1:p.Pro208Thr
XM_017010591.1:c.622C>A	XP_016866080.1:p.Pro208Thr
XM_017010592.2:c.622C>A	XP_016866081.1:p.Pro208Thr