Canonical Allele Identifier: CA1619759819

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842762A= , CM000668.2:g.32842762A=	GRCh38
NC_000006.11:g.32810539A= , CM000668.1:g.32810539A=	GRCh37
NC_000006.10:g.32918517A=	NCBI36
NG_009793.3:g.1009T=
NG_028165.1:g.7174T=
NG_009793.4:g.1009T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.496T=
ENST00000697612.1:n.1174T=
ENST00000374881.3:c.305T=	ENSP00000364015.2:p.Val102=
ENST00000374882.8:c.317T= MANE Select	ENSP00000364016.4:p.Val106=
ENST00000650411.1:n.1638T=
ENST00000650793.1:n.496T=
ENST00000374881.2:c.305T=	ENSP00000364015.2:p.Val102=
ENST00000374882.7:c.317T=	ENSP00000364016.3:p.Val106=
ENST00000395339.7:c.296-51T=	ENSP00000378748.3:n.296-51T=
ENST00000484003.1:n.701T=
NM_004159.4:c.305T=	NP_004150.1:p.Val102=
NM_148919.3:c.317T=	NP_683720.2:p.Val106=
NM_148919.4:c.317T= MANE Select	NP_683720.2:p.Val106=
NM_004159.5:c.305T=	NP_004150.1:p.Val102=