Canonical Allele Identifier: CA1619759794

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842715C= , CM000668.2:g.32842715C=	GRCh38
NC_000006.11:g.32810492C= , CM000668.1:g.32810492C=	GRCh37
NC_000006.10:g.32918470C=	NCBI36
NG_009793.3:g.1056G=
NG_028165.1:g.7221G=
NG_009793.4:g.1056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.543G=
ENST00000697612.1:n.1221G=
ENST00000374881.3:c.352G=	ENSP00000364015.2:p.Ala118=
ENST00000374882.8:c.364G= MANE Select	ENSP00000364016.4:p.Ala122=
ENST00000650411.1:n.1685G=
ENST00000650793.1:n.543G=
ENST00000374881.2:c.352G=	ENSP00000364015.2:p.Ala118=
ENST00000374882.7:c.364G=	ENSP00000364016.3:p.Ala122=
ENST00000395339.7:c.296-4G=	ENSP00000378748.3:n.296-4G=
ENST00000484003.1:n.748G=
NM_004159.4:c.352G=	NP_004150.1:p.Ala118=
NM_148919.3:c.364G=	NP_683720.2:p.Ala122=
NM_148919.4:c.364G= MANE Select	NP_683720.2:p.Ala122=
NM_004159.5:c.352G=	NP_004150.1:p.Ala118=