Canonical Allele Identifier: CA1619759778

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842686C= , CM000668.2:g.32842686C=	GRCh38
NC_000006.11:g.32810463C= , CM000668.1:g.32810463C=	GRCh37
NC_000006.10:g.32918441C=	NCBI36
NG_009793.3:g.1085G=
NG_028165.1:g.7250G=
NG_009793.4:g.1085G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.572G=
ENST00000697612.1:n.1250G=
ENST00000374881.3:c.381G=	ENSP00000364015.2:p.Leu127=
ENST00000374882.8:c.393G= MANE Select	ENSP00000364016.4:p.Leu131=
ENST00000650411.1:n.1714G=
ENST00000650793.1:n.572G=
ENST00000374881.2:c.381G=	ENSP00000364015.2:p.Leu127=
ENST00000374882.7:c.393G=	ENSP00000364016.3:p.Leu131=
ENST00000395339.7:c.321G=	ENSP00000378748.3:p.Leu107=
ENST00000484003.1:n.777G=
NM_004159.4:c.381G=	NP_004150.1:p.Leu127=
NM_148919.3:c.393G=	NP_683720.2:p.Leu131=
NM_148919.4:c.393G= MANE Select	NP_683720.2:p.Leu131=
NM_004159.5:c.381G=	NP_004150.1:p.Leu127=