Canonical Allele Identifier: CA363589546
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843053C>T , CM000668.2:g.32843053C>T GRCh38
NC_000006.11:g.32810830C>T , CM000668.1:g.32810830C>T GRCh37
NC_000006.10:g.32918808C>T NCBI36
NG_009793.3:g.718G>A
NG_028165.1:g.6883G>A
NG_009793.4:g.718G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000650793.2:n.205G>A
ENST00000697612.1:n.883G>A
ENST00000374881.3:c.172G>A ENSP00000364015.2:p.Glu58Lys
ENST00000374882.8:c.184G>A MANE Select ENSP00000364016.4:p.Glu62Lys
ENST00000650411.1:n.1505G>A
ENST00000650793.1:n.205G>A
ENST00000374881.2:c.172G>A ENSP00000364015.2:p.Glu58Lys
ENST00000374882.7:c.184G>A ENSP00000364016.3:p.Glu62Lys
ENST00000395339.7:c.184G>A ENSP00000378748.3:p.Glu62Lys
ENST00000484003.1:n.410G>A
NM_004159.4:c.172G>A NP_004150.1:p.Glu58Lys
NM_148919.3:c.184G>A NP_683720.2:p.Glu62Lys
NM_148919.4:c.184G>A MANE Select NP_683720.2:p.Glu62Lys
NM_004159.5:c.172G>A NP_004150.1:p.Glu58Lys