Canonical Allele Identifier: CA1619760045

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843071A= , CM000668.2:g.32843071A=	GRCh38
NC_000006.11:g.32810848A= , CM000668.1:g.32810848A=	GRCh37
NC_000006.10:g.32918826A=	NCBI36
NG_009793.3:g.700T=
NG_028165.1:g.6865T=
NG_009793.4:g.700T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.187T=
ENST00000697612.1:n.865T=
ENST00000374881.3:c.154T=	ENSP00000364015.2:p.Ser52=
ENST00000374882.8:c.166T= MANE Select	ENSP00000364016.4:p.Ser56=
ENST00000650411.1:n.1487T=
ENST00000650793.1:n.187T=
ENST00000374881.2:c.154T=	ENSP00000364015.2:p.Ser52=
ENST00000374882.7:c.166T=	ENSP00000364016.3:p.Ser56=
ENST00000395339.7:c.166T=	ENSP00000378748.3:p.Ser56=
ENST00000484003.1:n.392T=
NM_004159.4:c.154T=	NP_004150.1:p.Ser52=
NM_148919.3:c.166T=	NP_683720.2:p.Ser56=
NM_148919.4:c.166T= MANE Select	NP_683720.2:p.Ser56=
NM_004159.5:c.154T=	NP_004150.1:p.Ser52=