Canonical Allele Identifier: CA1619759804

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842731G= , CM000668.2:g.32842731G=	GRCh38
NC_000006.11:g.32810508G= , CM000668.1:g.32810508G=	GRCh37
NC_000006.10:g.32918486G=	NCBI36
NG_009793.3:g.1040C=
NG_028165.1:g.7205C=
NG_009793.4:g.1040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.527C=
ENST00000697612.1:n.1205C=
ENST00000374881.3:c.336C=	ENSP00000364015.2:p.Thr112=
ENST00000374882.8:c.348C= MANE Select	ENSP00000364016.4:p.Thr116=
ENST00000650411.1:n.1669C=
ENST00000650793.1:n.527C=
ENST00000374881.2:c.336C=	ENSP00000364015.2:p.Thr112=
ENST00000374882.7:c.348C=	ENSP00000364016.3:p.Thr116=
ENST00000395339.7:c.296-20C=	ENSP00000378748.3:n.296-20C=
ENST00000484003.1:n.732C=
NM_004159.4:c.336C=	NP_004150.1:p.Thr112=
NM_148919.3:c.348C=	NP_683720.2:p.Thr116=
NM_148919.4:c.348C= MANE Select	NP_683720.2:p.Thr116=
NM_004159.5:c.336C=	NP_004150.1:p.Thr112=