Canonical Allele Identifier: CA1671914669

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149378071A= , CM000668.2:g.149378071A=	GRCh38
NC_000006.11:g.149699207A= , CM000668.1:g.149699207A=	GRCh37
NC_000006.10:g.149740900A=	NCBI36
NG_021386.1:g.64772A=
NG_021386.2:g.165148A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000703212.1:n.571A=
ENST00000703213.1:c.156A=	ENSP00000515239.1:p.Arg52=
ENST00000636456.1:c.-96-601A=	ENSP00000490379.1:n.-96-601A=
ENST00000637181.2:c.156A= MANE Select	ENSP00000490618.1:p.Arg52=
ENST00000367456.5:c.156A=	ENSP00000356426.1:p.Arg52=
ENST00000470466.5:c.156A=	ENSP00000432709.1:p.Arg52=
ENST00000538427.5:c.156A=	ENSP00000445752.1:p.Arg52=
ENST00000606202.1:c.-67A=	ENSP00000476139.1:n.-67A=
NM_001292034.2:c.156A=	NP_001278963.1:p.Arg52=
NM_001292035.2:c.60A=	NP_001278964.1:p.Arg20=
NM_015093.5:c.156A=	NP_055908.1:p.Arg52=
XM_006715403.2:c.156A=	XP_006715466.1:p.Arg52=
XM_011535633.1:c.156A=	XP_011533935.1:p.Arg52=
XM_011535634.1:c.156A=	XP_011533936.1:p.Arg52=
XM_011535633.2:c.156A=	XP_011533935.1:p.Arg52=
XM_017010591.1:c.156A=	XP_016866080.1:p.Arg52=
XM_017010592.2:c.156A=	XP_016866081.1:p.Arg52=
NM_001292034.3:c.156A= MANE Select	NP_001278963.1:p.Arg52=
NM_001292035.3:c.60A=	NP_001278964.1:p.Arg20=
NM_001369506.1:c.156A=	NP_001356435.1:p.Arg52=
NM_015093.6:c.156A=	NP_055908.1:p.Arg52=