Canonical Allele Identifier: CA1619759767

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842665C= , CM000668.2:g.32842665C=	GRCh38
NC_000006.11:g.32810442C= , CM000668.1:g.32810442C=	GRCh37
NC_000006.10:g.32918420C=	NCBI36
NG_009793.3:g.1106G=
NG_028165.1:g.7271G=
NG_009793.4:g.1106G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.593G=
ENST00000697612.1:n.1264+7G=
ENST00000374881.3:c.395+7G=	ENSP00000364015.2:n.395+7G=
ENST00000374882.8:c.407+7G= MANE Select	ENSP00000364016.4:n.407+7G=
ENST00000650411.1:n.1728+7G=
ENST00000650793.1:n.593G=
ENST00000374881.2:c.395+7G=	ENSP00000364015.2:n.395+7G=
ENST00000374882.7:c.407+7G=	ENSP00000364016.3:n.407+7G=
ENST00000395339.7:c.335+7G=	ENSP00000378748.3:n.335+7G=
ENST00000484003.1:n.791+7G=
NM_004159.4:c.395+7G=	NP_004150.1:n.395+7G=
NM_148919.3:c.407+7G=	NP_683720.2:n.407+7G=
NM_148919.4:c.407+7G= MANE Select	NP_683720.2:n.407+7G=
NM_004159.5:c.395+7G=	NP_004150.1:n.395+7G=