Canonical Allele Identifier: CA2678184483

Gene: PSMB8

Linked Data

• gnomAD v4: 6-32842789-AGAAGATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842792_32842798del , CM000668.2:g.32842792_32842798del	GRCh38
NC_000006.11:g.32810569_32810575del , CM000668.1:g.32810569_32810575del	GRCh37
NC_000006.10:g.32918547_32918553del	NCBI36
NG_009793.3:g.975_981del
NG_028165.1:g.7140_7146del
NG_009793.4:g.975_981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.462_468del
ENST00000697612.1:n.1140_1146del
ENST00000374881.3:c.284-13_284-7del	ENSP00000364015.2:n.284-13_284-7del
ENST00000374882.8:c.296-13_296-7del MANE Select	ENSP00000364016.4:n.296-13_296-7del
ENST00000650411.1:n.1617-13_1617-7del
ENST00000650793.1:n.462_468del
ENST00000374881.2:c.284-13_284-7del	ENSP00000364015.2:n.284-13_284-7del
ENST00000374882.7:c.296-13_296-7del	ENSP00000364016.3:n.296-13_296-7del
ENST00000395339.7:c.296-85_296-79del	ENSP00000378748.3:n.296-85_296-79del
ENST00000484003.1:n.667_673del
NM_004159.4:c.284-13_284-7del	NP_004150.1:n.284-13_284-7del
NM_148919.3:c.296-13_296-7del	NP_683720.2:n.296-13_296-7del
NM_148919.4:c.296-13_296-7del MANE Select	NP_683720.2:n.296-13_296-7del
NM_004159.5:c.284-13_284-7del	NP_004150.1:n.284-13_284-7del