Canonical Allele Identifier: CA1619759790

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842710G= , CM000668.2:g.32842710G=	GRCh38
NC_000006.11:g.32810487G= , CM000668.1:g.32810487G=	GRCh37
NC_000006.10:g.32918465G=	NCBI36
NG_009793.3:g.1061C=
NG_028165.1:g.7226C=
NG_009793.4:g.1061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.548C=
ENST00000697612.1:n.1226C=
ENST00000374881.3:c.357C=	ENSP00000364015.2:p.Asp119=
ENST00000374882.8:c.369C= MANE Select	ENSP00000364016.4:p.Asp123=
ENST00000650411.1:n.1690C=
ENST00000650793.1:n.548C=
ENST00000374881.2:c.357C=	ENSP00000364015.2:p.Asp119=
ENST00000374882.7:c.369C=	ENSP00000364016.3:p.Asp123=
ENST00000395339.7:c.297C=	ENSP00000378748.3:p.Asn99=
ENST00000484003.1:n.753C=
NM_004159.4:c.357C=	NP_004150.1:p.Asp119=
NM_148919.3:c.369C=	NP_683720.2:p.Asp123=
NM_148919.4:c.369C= MANE Select	NP_683720.2:p.Asp123=
NM_004159.5:c.357C=	NP_004150.1:p.Asp119=