Canonical Allele Identifier: CA363589078
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32842681T>C , CM000668.2:g.32842681T>C GRCh38
NC_000006.11:g.32810458T>C , CM000668.1:g.32810458T>C GRCh37
NC_000006.10:g.32918436T>C NCBI36
NG_009793.3:g.1090A>G
NG_028165.1:g.7255A>G
NG_009793.4:g.1090A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.577A>G
ENST00000697612.1:n.1255A>G
ENST00000374881.3:c.386A>G ENSP00000364015.2:p.Lys129Arg
ENST00000374882.8:c.398A>G MANE Select ENSP00000364016.4:p.Lys133Arg
ENST00000650411.1:n.1719A>G
ENST00000650793.1:n.577A>G
ENST00000374881.2:c.386A>G ENSP00000364015.2:p.Lys129Arg
ENST00000374882.7:c.398A>G ENSP00000364016.3:p.Lys133Arg
ENST00000395339.7:c.326A>G ENSP00000378748.3:p.Lys109Arg
ENST00000484003.1:n.782A>G
NM_004159.4:c.386A>G NP_004150.1:p.Lys129Arg
NM_148919.3:c.398A>G NP_683720.2:p.Lys133Arg
NM_148919.4:c.398A>G MANE Select NP_683720.2:p.Lys133Arg
NM_004159.5:c.386A>G NP_004150.1:p.Lys129Arg