Canonical Allele Identifier: CA1671915914

Gene: TAB2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149379040T= , CM000668.2:g.149379040T=	GRCh38
NC_000006.11:g.149700176T= , CM000668.1:g.149700176T=	GRCh37
NC_000006.10:g.149741869T=	NCBI36
NG_021386.1:g.65741T=
NG_021386.2:g.166117T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703212.1:n.1540T=
ENST00000703213.1:c.1125T=	ENSP00000515239.1:p.Asn375=
ENST00000636456.1:c.273T=	ENSP00000490379.1:p.Asn91=
ENST00000637181.2:c.1125T= MANE Select	ENSP00000490618.1:p.Asn375=
ENST00000367456.5:c.1125T=	ENSP00000356426.1:p.Asn375=
ENST00000470466.5:c.1125T=	ENSP00000432709.1:p.Asn375=
ENST00000538427.5:c.1125T=	ENSP00000445752.1:p.Asn375=
NM_001292034.2:c.1125T=	NP_001278963.1:p.Asn375=
NM_001292035.2:c.1029T=	NP_001278964.1:p.Asn343=
NM_015093.5:c.1125T=	NP_055908.1:p.Asn375=
XM_006715403.2:c.1125T=	XP_006715466.1:p.Asn375=
XM_011535633.1:c.1125T=	XP_011533935.1:p.Asn375=
XM_011535634.1:c.1125T=	XP_011533936.1:p.Asn375=
XM_011535633.2:c.1125T=	XP_011533935.1:p.Asn375=
XM_017010591.1:c.1125T=	XP_016866080.1:p.Asn375=
XM_017010592.2:c.1125T=	XP_016866081.1:p.Asn375=
NM_001292034.3:c.1125T= MANE Select	NP_001278963.1:p.Asn375=
NM_001292035.3:c.1029T=	NP_001278964.1:p.Asn343=
NM_001369506.1:c.1125T=	NP_001356435.1:p.Asn375=
NM_015093.6:c.1125T=	NP_055908.1:p.Asn375=