Canonical Allele Identifier: CA1619759831

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842772C= , CM000668.2:g.32842772C=	GRCh38
NC_000006.11:g.32810549C= , CM000668.1:g.32810549C=	GRCh37
NC_000006.10:g.32918527C=	NCBI36
NG_009793.3:g.999G=
NG_028165.1:g.7164G=
NG_009793.4:g.999G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.486G=
ENST00000697612.1:n.1164G=
ENST00000374881.3:c.295G=	ENSP00000364015.2:p.Val99=
ENST00000374882.8:c.307G= MANE Select	ENSP00000364016.4:p.Val103=
ENST00000650411.1:n.1628G=
ENST00000650793.1:n.486G=
ENST00000374881.2:c.295G=	ENSP00000364015.2:p.Val99=
ENST00000374882.7:c.307G=	ENSP00000364016.3:p.Val103=
ENST00000395339.7:c.296-61G=	ENSP00000378748.3:n.296-61G=
ENST00000484003.1:n.691G=
NM_004159.4:c.295G=	NP_004150.1:p.Val99=
NM_148919.3:c.307G=	NP_683720.2:p.Val103=
NM_148919.4:c.307G= MANE Select	NP_683720.2:p.Val103=
NM_004159.5:c.295G=	NP_004150.1:p.Val99=