Canonical Allele Identifier: CA2678184861

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32843086-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843087_32843089del , CM000668.2:g.32843087_32843089del	GRCh38
NC_000006.11:g.32810864_32810866del , CM000668.1:g.32810864_32810866del	GRCh37
NC_000006.10:g.32918842_32918844del	NCBI36
NG_009793.3:g.682_684del
NG_028165.1:g.6847_6849del
NG_009793.4:g.682_684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.169_171del
ENST00000697612.1:n.847_849del
ENST00000374881.3:c.136_138del	ENSP00000364015.2:p.Pro46del
ENST00000374882.8:c.148_150del MANE Select	ENSP00000364016.4:p.Pro50del
ENST00000650411.1:n.1469_1471del
ENST00000650793.1:n.169_171del
ENST00000374881.2:c.136_138del	ENSP00000364015.2:p.Pro46del
ENST00000374882.7:c.148_150del	ENSP00000364016.3:p.Pro50del
ENST00000395339.7:c.148_150del	ENSP00000378748.3:p.Pro50del
ENST00000484003.1:n.374_376del
NM_004159.4:c.136_138del	NP_004150.1:p.Pro46del
NM_148919.3:c.148_150del	NP_683720.2:p.Pro50del
NM_148919.4:c.148_150del MANE Select	NP_683720.2:p.Pro50del
NM_004159.5:c.136_138del	NP_004150.1:p.Pro46del