Canonical Allele Identifier: CA1619759785

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842695C= , CM000668.2:g.32842695C=	GRCh38
NC_000006.11:g.32810472C= , CM000668.1:g.32810472C=	GRCh37
NC_000006.10:g.32918450C=	NCBI36
NG_009793.3:g.1076G=
NG_028165.1:g.7241G=
NG_009793.4:g.1076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.563G=
ENST00000697612.1:n.1241G=
ENST00000374881.3:c.372G=	ENSP00000364015.2:p.Glu124=
ENST00000374882.8:c.384G= MANE Select	ENSP00000364016.4:p.Glu128=
ENST00000650411.1:n.1705G=
ENST00000650793.1:n.563G=
ENST00000374881.2:c.372G=	ENSP00000364015.2:p.Glu124=
ENST00000374882.7:c.384G=	ENSP00000364016.3:p.Glu128=
ENST00000395339.7:c.312G=	ENSP00000378748.3:p.Glu104=
ENST00000484003.1:n.768G=
NM_004159.4:c.372G=	NP_004150.1:p.Glu124=
NM_148919.3:c.384G=	NP_683720.2:p.Glu128=
NM_148919.4:c.384G= MANE Select	NP_683720.2:p.Glu128=
NM_004159.5:c.372G=	NP_004150.1:p.Glu124=