Canonical Allele Identifier: CA1619760035

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843064C= , CM000668.2:g.32843064C=	GRCh38
NC_000006.11:g.32810841C= , CM000668.1:g.32810841C=	GRCh37
NC_000006.10:g.32918819C=	NCBI36
NG_009793.3:g.707G=
NG_028165.1:g.6872G=
NG_009793.4:g.707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.194G=
ENST00000697612.1:n.872G=
ENST00000374881.3:c.161G=	ENSP00000364015.2:p.Gly54=
ENST00000374882.8:c.173G= MANE Select	ENSP00000364016.4:p.Gly58=
ENST00000650411.1:n.1494G=
ENST00000650793.1:n.194G=
ENST00000374881.2:c.161G=	ENSP00000364015.2:p.Gly54=
ENST00000374882.7:c.173G=	ENSP00000364016.3:p.Gly58=
ENST00000395339.7:c.173G=	ENSP00000378748.3:p.Gly58=
ENST00000484003.1:n.399G=
NM_004159.4:c.161G=	NP_004150.1:p.Gly54=
NM_148919.3:c.173G=	NP_683720.2:p.Gly58=
NM_148919.4:c.173G= MANE Select	NP_683720.2:p.Gly58=
NM_004159.5:c.161G=	NP_004150.1:p.Gly54=