Canonical Allele Identifier: CA1619760038

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843067A= , CM000668.2:g.32843067A=	GRCh38
NC_000006.11:g.32810844A= , CM000668.1:g.32810844A=	GRCh37
NC_000006.10:g.32918822A=	NCBI36
NG_009793.3:g.704T=
NG_028165.1:g.6869T=
NG_009793.4:g.704T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.191T=
ENST00000697612.1:n.869T=
ENST00000374881.3:c.158T=	ENSP00000364015.2:p.Leu53=
ENST00000374882.8:c.170T= MANE Select	ENSP00000364016.4:p.Leu57=
ENST00000650411.1:n.1491T=
ENST00000650793.1:n.191T=
ENST00000374881.2:c.158T=	ENSP00000364015.2:p.Leu53=
ENST00000374882.7:c.170T=	ENSP00000364016.3:p.Leu57=
ENST00000395339.7:c.170T=	ENSP00000378748.3:p.Leu57=
ENST00000484003.1:n.396T=
NM_004159.4:c.158T=	NP_004150.1:p.Leu53=
NM_148919.3:c.170T=	NP_683720.2:p.Leu57=
NM_148919.4:c.170T= MANE Select	NP_683720.2:p.Leu57=
NM_004159.5:c.158T=	NP_004150.1:p.Leu53=