Canonical Allele Identifier: CA1619759977

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843005A= , CM000668.2:g.32843005A=	GRCh38
NC_000006.11:g.32810782A= , CM000668.1:g.32810782A=	GRCh37
NC_000006.10:g.32918760A=	NCBI36
NG_009793.3:g.766T=
NG_028165.1:g.6931T=
NG_009793.4:g.766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.253T=
ENST00000697612.1:n.931T=
ENST00000374881.3:c.220T=	ENSP00000364015.2:p.Phe74=
ENST00000374882.8:c.232T= MANE Select	ENSP00000364016.4:p.Phe78=
ENST00000650411.1:n.1553T=
ENST00000650793.1:n.253T=
ENST00000374881.2:c.220T=	ENSP00000364015.2:p.Phe74=
ENST00000374882.7:c.232T=	ENSP00000364016.3:p.Phe78=
ENST00000395339.7:c.232T=	ENSP00000378748.3:p.Phe78=
ENST00000484003.1:n.458T=
NM_004159.4:c.220T=	NP_004150.1:p.Phe74=
NM_148919.3:c.232T=	NP_683720.2:p.Phe78=
NM_148919.4:c.232T= MANE Select	NP_683720.2:p.Phe78=
NM_004159.5:c.220T=	NP_004150.1:p.Phe74=