Canonical Allele Identifier: CA1619760085

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843143C= , CM000668.2:g.32843143C=	GRCh38
NC_000006.11:g.32810920C= , CM000668.1:g.32810920C=	GRCh37
NC_000006.10:g.32918898C=	NCBI36
NG_009793.3:g.628G=
NG_028165.1:g.6793G=
NG_009793.4:g.628G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169-54G=
ENST00000697612.1:n.793G=
ENST00000374881.3:c.136-54G=	ENSP00000364015.2:n.136-54G=
ENST00000374882.8:c.148-54G= MANE Select	ENSP00000364016.4:n.148-54G=
ENST00000650411.1:n.1415G=
ENST00000650793.1:n.169-54G=
ENST00000374881.2:c.136-54G=	ENSP00000364015.2:n.136-54G=
ENST00000374882.7:c.148-54G=	ENSP00000364016.3:n.148-54G=
ENST00000395339.7:c.148-54G=	ENSP00000378748.3:n.148-54G=
ENST00000484003.1:n.374-54G=
NM_004159.4:c.136-54G=	NP_004150.1:n.136-54G=
NM_148919.3:c.148-54G=	NP_683720.2:n.148-54G=
NM_148919.4:c.148-54G= MANE Select	NP_683720.2:n.148-54G=
NM_004159.5:c.136-54G=	NP_004150.1:n.136-54G=