Canonical Allele Identifier: CA1619760005

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843028G= , CM000668.2:g.32843028G=	GRCh38
NC_000006.11:g.32810805G= , CM000668.1:g.32810805G=	GRCh37
NC_000006.10:g.32918783G=	NCBI36
NG_009793.3:g.743C=
NG_028165.1:g.6908C=
NG_009793.4:g.743C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.230C=
ENST00000697612.1:n.908C=
ENST00000374881.3:c.197C=	ENSP00000364015.2:p.Ala66=
ENST00000374882.8:c.209C= MANE Select	ENSP00000364016.4:p.Ala70=
ENST00000650411.1:n.1530C=
ENST00000650793.1:n.230C=
ENST00000374881.2:c.197C=	ENSP00000364015.2:p.Ala66=
ENST00000374882.7:c.209C=	ENSP00000364016.3:p.Ala70=
ENST00000395339.7:c.209C=	ENSP00000378748.3:p.Ala70=
ENST00000484003.1:n.435C=
NM_004159.4:c.197C=	NP_004150.1:p.Ala66=
NM_148919.3:c.209C=	NP_683720.2:p.Ala70=
NM_148919.4:c.209C= MANE Select	NP_683720.2:p.Ala70=
NM_004159.5:c.197C=	NP_004150.1:p.Ala66=