Canonical Allele Identifier: CA1619759825

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842766T= , CM000668.2:g.32842766T=	GRCh38
NC_000006.11:g.32810543T= , CM000668.1:g.32810543T=	GRCh37
NC_000006.10:g.32918521T=	NCBI36
NG_009793.3:g.1005A=
NG_028165.1:g.7170A=
NG_009793.4:g.1005A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.492A=
ENST00000697612.1:n.1170A=
ENST00000374881.3:c.301A=	ENSP00000364015.2:p.Lys101=
ENST00000374882.8:c.313A= MANE Select	ENSP00000364016.4:p.Lys105=
ENST00000650411.1:n.1634A=
ENST00000650793.1:n.492A=
ENST00000374881.2:c.301A=	ENSP00000364015.2:p.Lys101=
ENST00000374882.7:c.313A=	ENSP00000364016.3:p.Lys105=
ENST00000395339.7:c.296-55A=	ENSP00000378748.3:n.296-55A=
ENST00000484003.1:n.697A=
NM_004159.4:c.301A=	NP_004150.1:p.Lys101=
NM_148919.3:c.313A=	NP_683720.2:p.Lys105=
NM_148919.4:c.313A= MANE Select	NP_683720.2:p.Lys105=
NM_004159.5:c.301A=	NP_004150.1:p.Lys101=