Canonical Allele Identifier: CA1619759771

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842674G= , CM000668.2:g.32842674G=	GRCh38
NC_000006.11:g.32810451G= , CM000668.1:g.32810451G=	GRCh37
NC_000006.10:g.32918429G=	NCBI36
NG_009793.3:g.1097C=
NG_028165.1:g.7262C=
NG_009793.4:g.1097C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.584C=
ENST00000697612.1:n.1262C=
ENST00000374881.3:c.393C=	ENSP00000364015.2:p.Cys131=
ENST00000374882.8:c.405C= MANE Select	ENSP00000364016.4:p.Cys135=
ENST00000650411.1:n.1726C=
ENST00000650793.1:n.584C=
ENST00000374881.2:c.393C=	ENSP00000364015.2:p.Cys131=
ENST00000374882.7:c.405C=	ENSP00000364016.3:p.Cys135=
ENST00000395339.7:c.333C=	ENSP00000378748.3:p.Cys111=
ENST00000484003.1:n.789C=
NM_004159.4:c.393C=	NP_004150.1:p.Cys131=
NM_148919.3:c.405C=	NP_683720.2:p.Cys135=
NM_148919.4:c.405C= MANE Select	NP_683720.2:p.Cys135=
NM_004159.5:c.393C=	NP_004150.1:p.Cys131=