Canonical Allele Identifier: CA1619759934

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842947T= , CM000668.2:g.32842947T=	GRCh38
NC_000006.11:g.32810724T= , CM000668.1:g.32810724T=	GRCh37
NC_000006.10:g.32918702T=	NCBI36
NG_009793.3:g.824A=
NG_028165.1:g.6989A=
NG_009793.4:g.824A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.311A=
ENST00000697612.1:n.989A=
ENST00000374881.3:c.278A=	ENSP00000364015.2:p.Tyr93=
ENST00000374882.8:c.290A= MANE Select	ENSP00000364016.4:p.Tyr97=
ENST00000650411.1:n.1611A=
ENST00000650793.1:n.311A=
ENST00000374881.2:c.278A=	ENSP00000364015.2:p.Tyr93=
ENST00000374882.7:c.290A=	ENSP00000364016.3:p.Tyr97=
ENST00000395339.7:c.290A=	ENSP00000378748.3:p.Tyr97=
ENST00000484003.1:n.516A=
NM_004159.4:c.278A=	NP_004150.1:p.Tyr93=
NM_148919.3:c.290A=	NP_683720.2:p.Tyr97=
NM_148919.4:c.290A= MANE Select	NP_683720.2:p.Tyr97=
NM_004159.5:c.278A=	NP_004150.1:p.Tyr93=