Canonical Allele Identifier: CA363589082
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32842682T>G , CM000668.2:g.32842682T>G GRCh38
NC_000006.11:g.32810459T>G , CM000668.1:g.32810459T>G GRCh37
NC_000006.10:g.32918437T>G NCBI36
NG_009793.3:g.1089A>C
NG_028165.1:g.7254A>C
NG_009793.4:g.1089A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.576A>C
ENST00000697612.1:n.1254A>C
ENST00000374881.3:c.385A>C ENSP00000364015.2:p.Lys129Gln
ENST00000374882.8:c.397A>C MANE Select ENSP00000364016.4:p.Lys133Gln
ENST00000650411.1:n.1718A>C
ENST00000650793.1:n.576A>C
ENST00000374881.2:c.385A>C ENSP00000364015.2:p.Lys129Gln
ENST00000374882.7:c.397A>C ENSP00000364016.3:p.Lys133Gln
ENST00000395339.7:c.325A>C ENSP00000378748.3:p.Lys109Gln
ENST00000484003.1:n.781A>C
NM_004159.4:c.385A>C NP_004150.1:p.Lys129Gln
NM_148919.3:c.397A>C NP_683720.2:p.Lys133Gln
NM_148919.4:c.397A>C MANE Select NP_683720.2:p.Lys133Gln
NM_004159.5:c.385A>C NP_004150.1:p.Lys129Gln