Canonical Allele Identifier: CA2678184423

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842669-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842670del , CM000668.2:g.32842670del	GRCh38
NC_000006.11:g.32810447del , CM000668.1:g.32810447del	GRCh37
NC_000006.10:g.32918425del	NCBI36
NG_009793.3:g.1101del
NG_028165.1:g.7266del
NG_009793.4:g.1101del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.588del
ENST00000697612.1:n.1264+2del
ENST00000374881.3:c.395+2del	ENSP00000364015.2:n.395+2del
ENST00000374882.8:c.407+2del MANE Select	ENSP00000364016.4:n.407+2del
ENST00000650411.1:n.1728+2del
ENST00000650793.1:n.588del
ENST00000374881.2:c.395+2del	ENSP00000364015.2:n.395+2del
ENST00000374882.7:c.407+2del	ENSP00000364016.3:n.407+2del
ENST00000395339.7:c.335+2del	ENSP00000378748.3:n.335+2del
ENST00000484003.1:n.791+2del
NM_004159.4:c.395+2del	NP_004150.1:n.395+2del
NM_148919.3:c.407+2del	NP_683720.2:n.407+2del
NM_148919.4:c.407+2del MANE Select	NP_683720.2:n.407+2del
NM_004159.5:c.395+2del	NP_004150.1:n.395+2del