Canonical Allele Identifier: CA1619760527

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843852G= , CM000668.2:g.32843852G=	GRCh38
NC_000006.11:g.32811629G= , CM000668.1:g.32811629G=	GRCh37
NC_000006.10:g.32919607G=	NCBI36
NG_011759.1:g.15120C=
NG_028165.1:g.6084C=

Transcript Alleles

HGVS	Amino-acid Change
NM_148919.4:c.145C= MANE Select	NP_683720.2:p.Gln49=
ENST00000374882.8:c.145C= MANE Select	ENSP00000364016.4:p.Gln49=
NM_004159.4:c.135+427C=	NP_004150.1:n.135+427C=
NM_004159.5:c.135+427C=	NP_004150.1:n.135+427C=
NM_148919.3:c.145C=	NP_683720.2:p.Gln49=
ENST00000374881.2:c.135+427C=	ENSP00000364015.2:n.135+427C=
ENST00000374881.3:c.135+427C=	ENSP00000364015.2:n.135+427C=
ENST00000374882.7:c.145C=	ENSP00000364016.3:p.Gln49=
ENST00000395339.7:c.145C=	ENSP00000378748.3:p.Gln49=
ENST00000484003.1:n.373+427C=
ENST00000650411.1:n.706C=
ENST00000650793.1:n.166C=
ENST00000650793.2:n.166C=
ENST00000697612.1:n.84C=