Canonical Allele Identifier: CA1619759786

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842703A= , CM000668.2:g.32842703A=	GRCh38
NC_000006.11:g.32810480A= , CM000668.1:g.32810480A=	GRCh37
NC_000006.10:g.32918458A=	NCBI36
NG_009793.3:g.1068T=
NG_028165.1:g.7233T=
NG_009793.4:g.1068T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.555T=
ENST00000697612.1:n.1233T=
ENST00000374881.3:c.364T=	ENSP00000364015.2:p.Tyr122=
ENST00000374882.8:c.376T= MANE Select	ENSP00000364016.4:p.Tyr126=
ENST00000650411.1:n.1697T=
ENST00000650793.1:n.555T=
ENST00000374881.2:c.364T=	ENSP00000364015.2:p.Tyr122=
ENST00000374882.7:c.376T=	ENSP00000364016.3:p.Tyr126=
ENST00000395339.7:c.304T=	ENSP00000378748.3:p.Tyr102=
ENST00000484003.1:n.760T=
NM_004159.4:c.364T=	NP_004150.1:p.Tyr122=
NM_148919.3:c.376T=	NP_683720.2:p.Tyr126=
NM_148919.4:c.376T= MANE Select	NP_683720.2:p.Tyr126=
NM_004159.5:c.364T=	NP_004150.1:p.Tyr122=