Canonical Allele Identifier: CA464602484

Gene: VCP

Linked Data

• MyVariant Identifiers: chr9:g.35068013C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35068016C>A , CM000671.2:g.35068016C>A	GRCh38
NC_000009.11:g.35068013C>A , CM000671.1:g.35068013C>A	GRCh37
NC_000009.10:g.35058013C>A	NCBI36
NG_007887.1:g.9727G>T , LRG_657:g.9727G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.177G>T MANE Select	ENSP00000351777.6:p.Leu59=
ENST00000417448.2:c.42G>T	ENSP00000399456.2:p.Leu14=
ENST00000448530.6:c.42G>T	ENSP00000392088.2:p.Leu14=
ENST00000480327.2:n.449G>T
ENST00000676836.2:n.440G>T
ENST00000677257.1:c.171G>T	ENSP00000504354.1:p.Leu57=
ENST00000678018.1:c.*148G>T	ENSP00000503811.1:n.*148G>T
ENST00000678465.1:c.177G>T	ENSP00000504259.1:p.Leu59=
ENST00000678650.1:c.42G>T	ENSP00000503426.1:p.Leu14=
ENST00000679204.2:c.177G>T	ENSP00000503131.2:p.Leu59=
ENST00000679449.1:c.196G>T
ENST00000679599.1:n.447G>T
ENST00000679647.1:c.177G>T	ENSP00000506216.1:p.Leu59=
ENST00000679800.1:n.415G>T
ENST00000679862.1:c.42G>T	ENSP00000504990.1:p.Leu14=
ENST00000679902.1:c.177G>T	ENSP00000506338.1:p.Leu59=
ENST00000680079.1:c.*98G>T	ENSP00000506523.1:n.*98G>T
ENST00000680731.1:c.42G>T	ENSP00000505497.1:p.Leu14=
ENST00000680900.1:c.181G>T
ENST00000680916.1:c.177G>T	ENSP00000505769.1:p.Leu59=
ENST00000681335.1:c.177G>T	ENSP00000505230.1:p.Leu59=
ENST00000681386.1:c.42G>T	ENSP00000505509.1:p.Leu14=
ENST00000681690.1:n.449G>T
ENST00000681845.1:c.343G>T
ENST00000358901.10:c.177G>T	ENSP00000351777.6:p.Leu59=
ENST00000417448.1:c.42G>T	ENSP00000399456.1:p.Leu14=
ENST00000448530.5:c.42G>T	ENSP00000392088.1:p.Leu14=
ENST00000493886.5:n.373G>T
NM_007126.3:c.177G>T , LRG_657t1:c.177G>T	NP_009057.1:p.Leu59=
NM_001354927.1:c.42G>T	NP_001341856.1:p.Leu14=
NM_001354928.1:c.42G>T	NP_001341857.1:p.Leu14=
NM_007126.4:c.177G>T	NP_009057.1:p.Leu59=
NM_007126.5:c.177G>T MANE Select	NP_009057.1:p.Leu59=
NM_001354927.2:c.42G>T	NP_001341856.1:p.Leu14=
NM_001354928.2:c.42G>T	NP_001341857.1:p.Leu14=