Canonical Allele Identifier: CA1619759835

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842774C= , CM000668.2:g.32842774C=	GRCh38
NC_000006.11:g.32810551C= , CM000668.1:g.32810551C=	GRCh37
NC_000006.10:g.32918529C=	NCBI36
NG_009793.3:g.997G=
NG_028165.1:g.7162G=
NG_009793.4:g.997G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.484G=
ENST00000697612.1:n.1162G=
ENST00000374881.3:c.293G=	ENSP00000364015.2:p.Arg98=
ENST00000374882.8:c.305G= MANE Select	ENSP00000364016.4:p.Arg102=
ENST00000650411.1:n.1626G=
ENST00000650793.1:n.484G=
ENST00000374881.2:c.293G=	ENSP00000364015.2:p.Arg98=
ENST00000374882.7:c.305G=	ENSP00000364016.3:p.Arg102=
ENST00000395339.7:c.296-63G=	ENSP00000378748.3:n.296-63G=
ENST00000484003.1:n.689G=
NM_004159.4:c.293G=	NP_004150.1:p.Arg98=
NM_148919.3:c.305G=	NP_683720.2:p.Arg102=
NM_148919.4:c.305G= MANE Select	NP_683720.2:p.Arg102=
NM_004159.5:c.293G=	NP_004150.1:p.Arg98=