Canonical Allele Identifier: CA1619759855

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842822C= , CM000668.2:g.32842822C=	GRCh38
NC_000006.11:g.32810599C= , CM000668.1:g.32810599C=	GRCh37
NC_000006.10:g.32918577C=	NCBI36
NG_009793.3:g.949G=
NG_028165.1:g.7114G=
NG_009793.4:g.949G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.436G=
ENST00000697612.1:n.1114G=
ENST00000374881.3:c.284-39G=	ENSP00000364015.2:n.284-39G=
ENST00000374882.8:c.296-39G= MANE Select	ENSP00000364016.4:n.296-39G=
ENST00000650411.1:n.1617-39G=
ENST00000650793.1:n.436G=
ENST00000374881.2:c.284-39G=	ENSP00000364015.2:n.284-39G=
ENST00000374882.7:c.296-39G=	ENSP00000364016.3:n.296-39G=
ENST00000395339.7:c.296-111G=	ENSP00000378748.3:n.296-111G=
ENST00000484003.1:n.641G=
NM_004159.4:c.284-39G=	NP_004150.1:n.284-39G=
NM_148919.3:c.296-39G=	NP_683720.2:n.296-39G=
NM_148919.4:c.296-39G= MANE Select	NP_683720.2:n.296-39G=
NM_004159.5:c.284-39G=	NP_004150.1:n.284-39G=