Canonical Allele Identifier: CA2578579587
Gene: PSMB8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843153del , CM000668.2:g.32843153del GRCh38
NC_000006.11:g.32810930del , CM000668.1:g.32810930del GRCh37
NC_000006.10:g.32918908del NCBI36
NG_009793.3:g.621del
NG_028165.1:g.6786del
NG_009793.4:g.621del

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.169-61del
ENST00000697612.1:n.786del
ENST00000374881.3:c.136-61del ENSP00000364015.2:n.136-61del
ENST00000374882.8:c.148-61del MANE Select ENSP00000364016.4:n.148-61del
ENST00000650411.1:n.1408del
ENST00000650793.1:n.169-61del
ENST00000374881.2:c.136-61del ENSP00000364015.2:n.136-61del
ENST00000374882.7:c.148-61del ENSP00000364016.3:n.148-61del
ENST00000395339.7:c.148-61del ENSP00000378748.3:n.148-61del
ENST00000484003.1:n.374-61del
NM_004159.4:c.136-61del NP_004150.1:n.136-61del
NM_148919.3:c.148-61del NP_683720.2:n.148-61del
NM_148919.4:c.148-61del MANE Select NP_683720.2:n.148-61del
NM_004159.5:c.136-61del NP_004150.1:n.136-61del