Canonical Allele Identifier: CA1619759881

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842883T= , CM000668.2:g.32842883T=	GRCh38
NC_000006.11:g.32810660T= , CM000668.1:g.32810660T=	GRCh37
NC_000006.10:g.32918638T=	NCBI36
NG_009793.3:g.888A=
NG_028165.1:g.7053A=
NG_009793.4:g.888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.375A=
ENST00000697612.1:n.1053A=
ENST00000374881.3:c.283+59A=	ENSP00000364015.2:n.283+59A=
ENST00000374882.8:c.295+59A= MANE Select	ENSP00000364016.4:n.295+59A=
ENST00000650411.1:n.1616+59A=
ENST00000650793.1:n.375A=
ENST00000374881.2:c.283+59A=	ENSP00000364015.2:n.283+59A=
ENST00000374882.7:c.295+59A=	ENSP00000364016.3:n.295+59A=
ENST00000395339.7:c.295+59A=	ENSP00000378748.3:n.295+59A=
ENST00000484003.1:n.580A=
NM_004159.4:c.283+59A=	NP_004150.1:n.283+59A=
NM_148919.3:c.295+59A=	NP_683720.2:n.295+59A=
NM_148919.4:c.295+59A= MANE Select	NP_683720.2:n.295+59A=
NM_004159.5:c.283+59A=	NP_004150.1:n.283+59A=