Canonical Allele Identifier: CA863534454

Gene: VCP

Linked Data

• dbSNP Id: rs1451608363
• gnomAD v3: 9-35068140-CAGTAA-C
• gnomAD v4: 9-35068140-CAGTAA-C
• MyVariant Identifiers: chr9:g.35068138_35068142del (hg19) ; chr9:g.35068141_35068145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068142_35068146del , CM000671.2:g.35068142_35068146del	GRCh38
NC_000009.11:g.35068139_35068143del , CM000671.1:g.35068139_35068143del	GRCh37
NC_000009.10:g.35058139_35058143del	NCBI36
NG_007887.1:g.9598_9602del , LRG_657:g.9598_9602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.130-82_130-78del MANE Select	ENSP00000351777.6:n.130-82_130-78del
ENST00000417448.2:c.-6-82_-6-78del	ENSP00000399456.2:n.-6-82_-6-78del
ENST00000448530.6:c.-6-82_-6-78del	ENSP00000392088.2:n.-6-82_-6-78del
ENST00000480327.2:n.402-82_402-78del
ENST00000676836.2:n.393-82_393-78del
ENST00000677257.1:c.130-88_130-84del	ENSP00000504354.1:n.130-88_130-84del
ENST00000678018.1:c.*19_*23del	ENSP00000503811.1:n.*19_*23del
ENST00000678465.1:c.130-82_130-78del	ENSP00000504259.1:n.130-82_130-78del
ENST00000678650.1:c.-6-82_-6-78del	ENSP00000503426.1:n.-6-82_-6-78del
ENST00000679204.2:c.130-82_130-78del	ENSP00000503131.2:n.130-82_130-78del
ENST00000679449.1:c.113-46_113-42del
ENST00000679599.1:n.400-82_400-78del
ENST00000679647.1:c.130-82_130-78del	ENSP00000506216.1:n.130-82_130-78del
ENST00000679800.1:n.368-82_368-78del
ENST00000679862.1:c.-6-82_-6-78del	ENSP00000504990.1:n.-6-82_-6-78del
ENST00000679902.1:c.130-82_130-78del	ENSP00000506338.1:n.130-82_130-78del
ENST00000680079.1:c.*51-82_*51-78del	ENSP00000506523.1:n.*51-82_*51-78del
ENST00000680900.1:c.113-61_113-57del
ENST00000680916.1:c.130-82_130-78del	ENSP00000505769.1:n.130-82_130-78del
ENST00000681335.1:c.130-82_130-78del	ENSP00000505230.1:n.130-82_130-78del
ENST00000681386.1:c.-6-82_-6-78del	ENSP00000505509.1:n.-6-82_-6-78del
ENST00000681690.1:n.402-82_402-78del
ENST00000681845.1:c.296-82_296-78del
ENST00000358901.10:c.130-82_130-78del	ENSP00000351777.6:n.130-82_130-78del
ENST00000417448.1:c.-6-82_-6-78del	ENSP00000399456.1:n.-6-82_-6-78del
ENST00000448530.5:c.-6-82_-6-78del	ENSP00000392088.1:n.-6-82_-6-78del
ENST00000493886.5:n.326-82_326-78del
NM_007126.3:c.130-82_130-78del , LRG_657t1:c.130-82_130-78del	NP_009057.1:n.130-82_130-78del
NM_001354927.1:c.-6-82_-6-78del	NP_001341856.1:n.-6-82_-6-78del
NM_001354928.1:c.-6-82_-6-78del	NP_001341857.1:n.-6-82_-6-78del
NM_007126.4:c.130-82_130-78del	NP_009057.1:n.130-82_130-78del
NM_007126.5:c.130-82_130-78del MANE Select	NP_009057.1:n.130-82_130-78del
NM_001354927.2:c.-6-82_-6-78del	NP_001341856.1:n.-6-82_-6-78del
NM_001354928.2:c.-6-82_-6-78del	NP_001341857.1:n.-6-82_-6-78del