Canonical Allele Identifier: CA1671916048

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149379119C= , CM000668.2:g.149379119C=	GRCh38
NC_000006.11:g.149700255C= , CM000668.1:g.149700255C=	GRCh37
NC_000006.10:g.149741948C=	NCBI36
NG_021386.1:g.65820C=
NG_021386.2:g.166196C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.1619C=
ENST00000703213.1:c.1204C=	ENSP00000515239.1:p.Arg402=
ENST00000636456.1:c.352C=	ENSP00000490379.1:p.Arg118=
ENST00000637181.2:c.1204C= MANE Select	ENSP00000490618.1:p.Arg402=
ENST00000367456.5:c.1204C=	ENSP00000356426.1:p.Arg402=
ENST00000470466.5:c.1204C=	ENSP00000432709.1:p.Arg402=
ENST00000538427.5:c.1204C=	ENSP00000445752.1:p.Arg402=
NM_001292034.2:c.1204C=	NP_001278963.1:p.Arg402=
NM_001292035.2:c.1108C=	NP_001278964.1:p.Arg370=
NM_015093.5:c.1204C=	NP_055908.1:p.Arg402=
XM_006715403.2:c.1204C=	XP_006715466.1:p.Arg402=
XM_011535633.1:c.1204C=	XP_011533935.1:p.Arg402=
XM_011535634.1:c.1204C=	XP_011533936.1:p.Arg402=
XM_011535633.2:c.1204C=	XP_011533935.1:p.Arg402=
XM_017010591.1:c.1204C=	XP_016866080.1:p.Arg402=
XM_017010592.2:c.1204C=	XP_016866081.1:p.Arg402=
NM_001292034.3:c.1204C= MANE Select	NP_001278963.1:p.Arg402=
NM_001292035.3:c.1108C=	NP_001278964.1:p.Arg370=
NM_001369506.1:c.1204C=	NP_001356435.1:p.Arg402=
NM_015093.6:c.1204C=	NP_055908.1:p.Arg402=