Canonical Allele Identifier: CA1619759970

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842998A= , CM000668.2:g.32842998A=	GRCh38
NC_000006.11:g.32810775A= , CM000668.1:g.32810775A=	GRCh37
NC_000006.10:g.32918753A=	NCBI36
NG_009793.3:g.773T=
NG_028165.1:g.6938T=
NG_009793.4:g.773T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.260T=
ENST00000697612.1:n.938T=
ENST00000374881.3:c.227T=	ENSP00000364015.2:p.Phe76=
ENST00000374882.8:c.239T= MANE Select	ENSP00000364016.4:p.Phe80=
ENST00000650411.1:n.1560T=
ENST00000650793.1:n.260T=
ENST00000374881.2:c.227T=	ENSP00000364015.2:p.Phe76=
ENST00000374882.7:c.239T=	ENSP00000364016.3:p.Phe80=
ENST00000395339.7:c.239T=	ENSP00000378748.3:p.Phe80=
ENST00000484003.1:n.465T=
NM_004159.4:c.227T=	NP_004150.1:p.Phe76=
NM_148919.3:c.239T=	NP_683720.2:p.Phe80=
NM_148919.4:c.239T= MANE Select	NP_683720.2:p.Phe80=
NM_004159.5:c.227T=	NP_004150.1:p.Phe76=