Canonical Allele Identifier: CA1619760077

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843129T= , CM000668.2:g.32843129T=	GRCh38
NC_000006.11:g.32810906T= , CM000668.1:g.32810906T=	GRCh37
NC_000006.10:g.32918884T=	NCBI36
NG_009793.3:g.642A=
NG_028165.1:g.6807A=
NG_009793.4:g.642A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-40A=
ENST00000697612.1:n.807A=
ENST00000374881.3:c.136-40A=	ENSP00000364015.2:n.136-40A=
ENST00000374882.8:c.148-40A= MANE Select	ENSP00000364016.4:n.148-40A=
ENST00000650411.1:n.1429A=
ENST00000650793.1:n.169-40A=
ENST00000374881.2:c.136-40A=	ENSP00000364015.2:n.136-40A=
ENST00000374882.7:c.148-40A=	ENSP00000364016.3:n.148-40A=
ENST00000395339.7:c.148-40A=	ENSP00000378748.3:n.148-40A=
ENST00000484003.1:n.374-40A=
NM_004159.4:c.136-40A=	NP_004150.1:n.136-40A=
NM_148919.3:c.148-40A=	NP_683720.2:n.148-40A=
NM_148919.4:c.148-40A= MANE Select	NP_683720.2:n.148-40A=
NM_004159.5:c.136-40A=	NP_004150.1:n.136-40A=