Canonical Allele Identifier: CA1619759797

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842721A= , CM000668.2:g.32842721A=	GRCh38
NC_000006.11:g.32810498A= , CM000668.1:g.32810498A=	GRCh37
NC_000006.10:g.32918476A=	NCBI36
NG_009793.3:g.1050T=
NG_028165.1:g.7215T=
NG_009793.4:g.1050T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.537T=
ENST00000697612.1:n.1215T=
ENST00000374881.3:c.346T=	ENSP00000364015.2:p.Cys116=
ENST00000374882.8:c.358T= MANE Select	ENSP00000364016.4:p.Cys120=
ENST00000650411.1:n.1679T=
ENST00000650793.1:n.537T=
ENST00000374881.2:c.346T=	ENSP00000364015.2:p.Cys116=
ENST00000374882.7:c.358T=	ENSP00000364016.3:p.Cys120=
ENST00000395339.7:c.296-10T=	ENSP00000378748.3:n.296-10T=
ENST00000484003.1:n.742T=
NM_004159.4:c.346T=	NP_004150.1:p.Cys116=
NM_148919.3:c.358T=	NP_683720.2:p.Cys120=
NM_148919.4:c.358T= MANE Select	NP_683720.2:p.Cys120=
NM_004159.5:c.346T=	NP_004150.1:p.Cys116=