Canonical Allele Identifier: CA2579329628

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068077_35068079del , CM000671.2:g.35068077_35068079del	GRCh38
NC_000009.11:g.35068074_35068076del , CM000671.1:g.35068074_35068076del	GRCh37
NC_000009.10:g.35058074_35058076del	NCBI36
NG_007887.1:g.9664_9666del , LRG_657:g.9664_9666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.130-16_130-14del MANE Select	ENSP00000351777.6:n.130-16_130-14del
ENST00000417448.2:c.-6-16_-6-14del	ENSP00000399456.2:n.-6-16_-6-14del
ENST00000448530.6:c.-6-16_-6-14del	ENSP00000392088.2:n.-6-16_-6-14del
ENST00000480327.2:n.402-16_402-14del
ENST00000676836.2:n.393-16_393-14del
ENST00000677257.1:c.130-22_130-20del	ENSP00000504354.1:n.130-22_130-20del
ENST00000678018.1:c.*85_*87del	ENSP00000503811.1:n.*85_*87del
ENST00000678465.1:c.130-16_130-14del	ENSP00000504259.1:n.130-16_130-14del
ENST00000678650.1:c.-6-16_-6-14del	ENSP00000503426.1:n.-6-16_-6-14del
ENST00000679204.2:c.130-16_130-14del	ENSP00000503131.2:n.130-16_130-14del
ENST00000679449.1:c.133_135del
ENST00000679599.1:n.400-16_400-14del
ENST00000679647.1:c.130-16_130-14del	ENSP00000506216.1:n.130-16_130-14del
ENST00000679800.1:n.368-16_368-14del
ENST00000679862.1:c.-6-16_-6-14del	ENSP00000504990.1:n.-6-16_-6-14del
ENST00000679902.1:c.130-16_130-14del	ENSP00000506338.1:n.130-16_130-14del
ENST00000680079.1:c.*51-16_*51-14del	ENSP00000506523.1:n.*51-16_*51-14del
ENST00000680900.1:c.118_120del
ENST00000680916.1:c.130-16_130-14del	ENSP00000505769.1:n.130-16_130-14del
ENST00000681335.1:c.130-16_130-14del	ENSP00000505230.1:n.130-16_130-14del
ENST00000681386.1:c.-6-16_-6-14del	ENSP00000505509.1:n.-6-16_-6-14del
ENST00000681690.1:n.402-16_402-14del
ENST00000681845.1:c.296-16_296-14del
ENST00000358901.10:c.130-16_130-14del	ENSP00000351777.6:n.130-16_130-14del
ENST00000417448.1:c.-6-16_-6-14del	ENSP00000399456.1:n.-6-16_-6-14del
ENST00000448530.5:c.-6-16_-6-14del	ENSP00000392088.1:n.-6-16_-6-14del
ENST00000493886.5:n.326-16_326-14del
NM_007126.3:c.130-16_130-14del , LRG_657t1:c.130-16_130-14del	NP_009057.1:n.130-16_130-14del
NM_001354927.1:c.-6-16_-6-14del	NP_001341856.1:n.-6-16_-6-14del
NM_001354928.1:c.-6-16_-6-14del	NP_001341857.1:n.-6-16_-6-14del
NM_007126.4:c.130-16_130-14del	NP_009057.1:n.130-16_130-14del
NM_007126.5:c.130-16_130-14del MANE Select	NP_009057.1:n.130-16_130-14del
NM_001354927.2:c.-6-16_-6-14del	NP_001341856.1:n.-6-16_-6-14del
NM_001354928.2:c.-6-16_-6-14del	NP_001341857.1:n.-6-16_-6-14del