Canonical Allele Identifier: CA1619759951

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842965C= , CM000668.2:g.32842965C=	GRCh38
NC_000006.11:g.32810742C= , CM000668.1:g.32810742C=	GRCh37
NC_000006.10:g.32918720C=	NCBI36
NG_009793.3:g.806G=
NG_028165.1:g.6971G=
NG_009793.4:g.806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.293G=
ENST00000697612.1:n.971G=
ENST00000374881.3:c.260G=	ENSP00000364015.2:p.Arg87=
ENST00000374882.8:c.272G= MANE Select	ENSP00000364016.4:p.Arg91=
ENST00000650411.1:n.1593G=
ENST00000650793.1:n.293G=
ENST00000374881.2:c.260G=	ENSP00000364015.2:p.Arg87=
ENST00000374882.7:c.272G=	ENSP00000364016.3:p.Arg91=
ENST00000395339.7:c.272G=	ENSP00000378748.3:p.Arg91=
ENST00000484003.1:n.498G=
NM_004159.4:c.260G=	NP_004150.1:p.Arg87=
NM_148919.3:c.272G=	NP_683720.2:p.Arg91=
NM_148919.4:c.272G= MANE Select	NP_683720.2:p.Arg91=
NM_004159.5:c.260G=	NP_004150.1:p.Arg87=