Canonical Allele Identifier: CA363589074

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842679-C-T
• COSMIC: COSM6396866 ; COSM6396867
• MyVariant Identifiers: chr6:g.32810456C>T (hg19) ; chr6:g.32842679C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842679C>T , CM000668.2:g.32842679C>T	GRCh38
NC_000006.11:g.32810456C>T , CM000668.1:g.32810456C>T	GRCh37
NC_000006.10:g.32918434C>T	NCBI36
NG_009793.3:g.1092G>A
NG_028165.1:g.7257G>A
NG_009793.4:g.1092G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.579G>A
ENST00000697612.1:n.1257G>A
ENST00000374881.3:c.388G>A	ENSP00000364015.2:p.Glu130Lys
ENST00000374882.8:c.400G>A MANE Select	ENSP00000364016.4:p.Glu134Lys
ENST00000650411.1:n.1721G>A
ENST00000650793.1:n.579G>A
ENST00000374881.2:c.388G>A	ENSP00000364015.2:p.Glu130Lys
ENST00000374882.7:c.400G>A	ENSP00000364016.3:p.Glu134Lys
ENST00000395339.7:c.328G>A	ENSP00000378748.3:p.Glu110Lys
ENST00000484003.1:n.784G>A
NM_004159.4:c.388G>A	NP_004150.1:p.Glu130Lys
NM_148919.3:c.400G>A	NP_683720.2:p.Glu134Lys
NM_148919.4:c.400G>A MANE Select	NP_683720.2:p.Glu134Lys
NM_004159.5:c.388G>A	NP_004150.1:p.Glu130Lys