Canonical Allele Identifier: CA1619759791

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842712C= , CM000668.2:g.32842712C=	GRCh38
NC_000006.11:g.32810489C= , CM000668.1:g.32810489C=	GRCh37
NC_000006.10:g.32918467C=	NCBI36
NG_009793.3:g.1059G=
NG_028165.1:g.7224G=
NG_009793.4:g.1059G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.546G=
ENST00000697612.1:n.1224G=
ENST00000374881.3:c.355G=	ENSP00000364015.2:p.Asp119=
ENST00000374882.8:c.367G= MANE Select	ENSP00000364016.4:p.Asp123=
ENST00000650411.1:n.1688G=
ENST00000650793.1:n.546G=
ENST00000374881.2:c.355G=	ENSP00000364015.2:p.Asp119=
ENST00000374882.7:c.367G=	ENSP00000364016.3:p.Asp123=
ENST00000395339.7:c.296-1G=	ENSP00000378748.3:n.296-1G=
ENST00000484003.1:n.751G=
NM_004159.4:c.355G=	NP_004150.1:p.Asp119=
NM_148919.3:c.367G=	NP_683720.2:p.Asp123=
NM_148919.4:c.367G= MANE Select	NP_683720.2:p.Asp123=
NM_004159.5:c.355G=	NP_004150.1:p.Asp119=