Canonical Allele Identifier: CA1619759972

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843003G= , CM000668.2:g.32843003G=	GRCh38
NC_000006.11:g.32810780G= , CM000668.1:g.32810780G=	GRCh37
NC_000006.10:g.32918758G=	NCBI36
NG_009793.3:g.768C=
NG_028165.1:g.6933C=
NG_009793.4:g.768C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.255C=
ENST00000697612.1:n.933C=
ENST00000374881.3:c.222C=	ENSP00000364015.2:p.Phe74=
ENST00000374882.8:c.234C= MANE Select	ENSP00000364016.4:p.Phe78=
ENST00000650411.1:n.1555C=
ENST00000650793.1:n.255C=
ENST00000374881.2:c.222C=	ENSP00000364015.2:p.Phe74=
ENST00000374882.7:c.234C=	ENSP00000364016.3:p.Phe78=
ENST00000395339.7:c.234C=	ENSP00000378748.3:p.Phe78=
ENST00000484003.1:n.460C=
NM_004159.4:c.222C=	NP_004150.1:p.Phe74=
NM_148919.3:c.234C=	NP_683720.2:p.Phe78=
NM_148919.4:c.234C= MANE Select	NP_683720.2:p.Phe78=
NM_004159.5:c.222C=	NP_004150.1:p.Phe74=