Canonical Allele Identifier: CA1619759849

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842812A= , CM000668.2:g.32842812A=	GRCh38
NC_000006.11:g.32810589A= , CM000668.1:g.32810589A=	GRCh37
NC_000006.10:g.32918567A=	NCBI36
NG_009793.3:g.959T=
NG_028165.1:g.7124T=
NG_009793.4:g.959T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.446T=
ENST00000697612.1:n.1124T=
ENST00000374881.3:c.284-29T=	ENSP00000364015.2:n.284-29T=
ENST00000374882.8:c.296-29T= MANE Select	ENSP00000364016.4:n.296-29T=
ENST00000650411.1:n.1617-29T=
ENST00000650793.1:n.446T=
ENST00000374881.2:c.284-29T=	ENSP00000364015.2:n.284-29T=
ENST00000374882.7:c.296-29T=	ENSP00000364016.3:n.296-29T=
ENST00000395339.7:c.296-101T=	ENSP00000378748.3:n.296-101T=
ENST00000484003.1:n.651T=
NM_004159.4:c.284-29T=	NP_004150.1:n.284-29T=
NM_148919.3:c.296-29T=	NP_683720.2:n.296-29T=
NM_148919.4:c.296-29T= MANE Select	NP_683720.2:n.296-29T=
NM_004159.5:c.284-29T=	NP_004150.1:n.284-29T=