Canonical Allele Identifier: CA1619759747

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842631A= , CM000668.2:g.32842631A=	GRCh38
NC_000006.11:g.32810408A= , CM000668.1:g.32810408A=	GRCh37
NC_000006.10:g.32918386A=	NCBI36
NG_009793.3:g.1140T=
NG_028165.1:g.7305T=
NG_009793.4:g.1140T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.627T=
ENST00000697612.1:n.1264+41T=
ENST00000374881.3:c.395+41T=	ENSP00000364015.2:n.395+41T=
ENST00000374882.8:c.407+41T= MANE Select	ENSP00000364016.4:n.407+41T=
ENST00000650411.1:n.1728+41T=
ENST00000650793.1:n.627T=
ENST00000374881.2:c.395+41T=	ENSP00000364015.2:n.395+41T=
ENST00000374882.7:c.407+41T=	ENSP00000364016.3:n.407+41T=
ENST00000395339.7:c.335+41T=	ENSP00000378748.3:n.335+41T=
ENST00000484003.1:n.791+41T=
NM_004159.4:c.395+41T=	NP_004150.1:n.395+41T=
NM_148919.3:c.407+41T=	NP_683720.2:n.407+41T=
NM_148919.4:c.407+41T= MANE Select	NP_683720.2:n.407+41T=
NM_004159.5:c.395+41T=	NP_004150.1:n.395+41T=