Canonical Allele Identifier: CA1619759773

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842675C= , CM000668.2:g.32842675C=	GRCh38
NC_000006.11:g.32810452C= , CM000668.1:g.32810452C=	GRCh37
NC_000006.10:g.32918430C=	NCBI36
NG_009793.3:g.1096G=
NG_028165.1:g.7261G=
NG_009793.4:g.1096G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.583G=
ENST00000697612.1:n.1261G=
ENST00000374881.3:c.392G=	ENSP00000364015.2:p.Cys131=
ENST00000374882.8:c.404G= MANE Select	ENSP00000364016.4:p.Cys135=
ENST00000650411.1:n.1725G=
ENST00000650793.1:n.583G=
ENST00000374881.2:c.392G=	ENSP00000364015.2:p.Cys131=
ENST00000374882.7:c.404G=	ENSP00000364016.3:p.Cys135=
ENST00000395339.7:c.332G=	ENSP00000378748.3:p.Cys111=
ENST00000484003.1:n.788G=
NM_004159.4:c.392G=	NP_004150.1:p.Cys131=
NM_148919.3:c.404G=	NP_683720.2:p.Cys135=
NM_148919.4:c.404G= MANE Select	NP_683720.2:p.Cys135=
NM_004159.5:c.392G=	NP_004150.1:p.Cys131=