Canonical Allele Identifier: CA2578579577

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842834del , CM000668.2:g.32842834del	GRCh38
NC_000006.11:g.32810611del , CM000668.1:g.32810611del	GRCh37
NC_000006.10:g.32918589del	NCBI36
NG_009793.3:g.941del
NG_028165.1:g.7106del
NG_009793.4:g.941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.428del
ENST00000697612.1:n.1106del
ENST00000374881.3:c.284-47del	ENSP00000364015.2:n.284-47del
ENST00000374882.8:c.296-47del MANE Select	ENSP00000364016.4:n.296-47del
ENST00000650411.1:n.1617-47del
ENST00000650793.1:n.428del
ENST00000374881.2:c.284-47del	ENSP00000364015.2:n.284-47del
ENST00000374882.7:c.296-47del	ENSP00000364016.3:n.296-47del
ENST00000395339.7:c.295+112del	ENSP00000378748.3:n.295+112del
ENST00000484003.1:n.633del
NM_004159.4:c.284-47del	NP_004150.1:n.284-47del
NM_148919.3:c.296-47del	NP_683720.2:n.296-47del
NM_148919.4:c.296-47del MANE Select	NP_683720.2:n.296-47del
NM_004159.5:c.284-47del	NP_004150.1:n.284-47del