Canonical Allele Identifier: CA2719530609

Gene: VCP

Linked Data

• dbSNP Id: rs2131040743

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068070_35068071insC , CM000671.2:g.35068070_35068071insC	GRCh38
NC_000009.11:g.35068067_35068068insC , CM000671.1:g.35068067_35068068insC	GRCh37
NC_000009.10:g.35058067_35058068insC	NCBI36
NG_007887.1:g.9672_9673insG , LRG_657:g.9672_9673insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.130-8_130-7insG MANE Select	ENSP00000351777.6:n.130-8_130-7insG
ENST00000417448.2:c.-6-8_-6-7insG	ENSP00000399456.2:n.-6-8_-6-7insG
ENST00000448530.6:c.-6-8_-6-7insG	ENSP00000392088.2:n.-6-8_-6-7insG
ENST00000480327.2:n.402-8_402-7insG
ENST00000676836.2:n.393-8_393-7insG
ENST00000677257.1:c.130-14_130-13insG	ENSP00000504354.1:n.130-14_130-13insG
ENST00000678018.1:c.*93_*94insG	ENSP00000503811.1:n.*93_*94insG
ENST00000678465.1:c.130-8_130-7insG	ENSP00000504259.1:n.130-8_130-7insG
ENST00000678650.1:c.-6-8_-6-7insG	ENSP00000503426.1:n.-6-8_-6-7insG
ENST00000679204.2:c.130-8_130-7insG	ENSP00000503131.2:n.130-8_130-7insG
ENST00000679449.1:c.141_142insG
ENST00000679599.1:n.400-8_400-7insG
ENST00000679647.1:c.130-8_130-7insG	ENSP00000506216.1:n.130-8_130-7insG
ENST00000679800.1:n.368-8_368-7insG
ENST00000679862.1:c.-6-8_-6-7insG	ENSP00000504990.1:n.-6-8_-6-7insG
ENST00000679902.1:c.130-8_130-7insG	ENSP00000506338.1:n.130-8_130-7insG
ENST00000680079.1:c.*51-8_*51-7insG	ENSP00000506523.1:n.*51-8_*51-7insG
ENST00000680900.1:c.126_127insG
ENST00000680916.1:c.130-8_130-7insG	ENSP00000505769.1:n.130-8_130-7insG
ENST00000681335.1:c.130-8_130-7insG	ENSP00000505230.1:n.130-8_130-7insG
ENST00000681386.1:c.-6-8_-6-7insG	ENSP00000505509.1:n.-6-8_-6-7insG
ENST00000681690.1:n.402-8_402-7insG
ENST00000681845.1:c.296-8_296-7insG
ENST00000358901.10:c.130-8_130-7insG	ENSP00000351777.6:n.130-8_130-7insG
ENST00000417448.1:c.-6-8_-6-7insG	ENSP00000399456.1:n.-6-8_-6-7insG
ENST00000448530.5:c.-6-8_-6-7insG	ENSP00000392088.1:n.-6-8_-6-7insG
ENST00000493886.5:n.326-8_326-7insG
NM_007126.3:c.130-8_130-7insG , LRG_657t1:c.130-8_130-7insG	NP_009057.1:n.130-8_130-7insG
NM_001354927.1:c.-6-8_-6-7insG	NP_001341856.1:n.-6-8_-6-7insG
NM_001354928.1:c.-6-8_-6-7insG	NP_001341857.1:n.-6-8_-6-7insG
NM_007126.4:c.130-8_130-7insG	NP_009057.1:n.130-8_130-7insG
NM_007126.5:c.130-8_130-7insG MANE Select	NP_009057.1:n.130-8_130-7insG
NM_001354927.2:c.-6-8_-6-7insG	NP_001341856.1:n.-6-8_-6-7insG
NM_001354928.2:c.-6-8_-6-7insG	NP_001341857.1:n.-6-8_-6-7insG