Canonical Allele Identifier: CA1619759789
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32842709A= , CM000668.2:g.32842709A= GRCh38
NC_000006.11:g.32810486A= , CM000668.1:g.32810486A= GRCh37
NC_000006.10:g.32918464A= NCBI36
NG_009793.3:g.1062T=
NG_028165.1:g.7227T=
NG_009793.4:g.1062T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.549T=
ENST00000697612.1:n.1227T=
ENST00000374881.3:c.358T= ENSP00000364015.2:p.Cys120=
ENST00000374882.8:c.370T= MANE Select ENSP00000364016.4:p.Cys124=
ENST00000650411.1:n.1691T=
ENST00000650793.1:n.549T=
ENST00000374881.2:c.358T= ENSP00000364015.2:p.Cys120=
ENST00000374882.7:c.370T= ENSP00000364016.3:p.Cys124=
ENST00000395339.7:c.298T= ENSP00000378748.3:p.Cys100=
ENST00000484003.1:n.754T=
NM_004159.4:c.358T= NP_004150.1:p.Cys120=
NM_148919.3:c.370T= NP_683720.2:p.Cys124=
NM_148919.4:c.370T= MANE Select NP_683720.2:p.Cys124=
NM_004159.5:c.358T= NP_004150.1:p.Cys120=