Canonical Allele Identifier: CA1619759805

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842732G= , CM000668.2:g.32842732G=	GRCh38
NC_000006.11:g.32810509G= , CM000668.1:g.32810509G=	GRCh37
NC_000006.10:g.32918487G=	NCBI36
NG_009793.3:g.1039C=
NG_028165.1:g.7204C=
NG_009793.4:g.1039C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.526C=
ENST00000697612.1:n.1204C=
ENST00000374881.3:c.335C=	ENSP00000364015.2:p.Thr112=
ENST00000374882.8:c.347C= MANE Select	ENSP00000364016.4:p.Thr116=
ENST00000650411.1:n.1668C=
ENST00000650793.1:n.526C=
ENST00000374881.2:c.335C=	ENSP00000364015.2:p.Thr112=
ENST00000374882.7:c.347C=	ENSP00000364016.3:p.Thr116=
ENST00000395339.7:c.296-21C=	ENSP00000378748.3:n.296-21C=
ENST00000484003.1:n.731C=
NM_004159.4:c.335C=	NP_004150.1:p.Thr112=
NM_148919.3:c.347C=	NP_683720.2:p.Thr116=
NM_148919.4:c.347C= MANE Select	NP_683720.2:p.Thr116=
NM_004159.5:c.335C=	NP_004150.1:p.Thr112=