Canonical Allele Identifier: CA373294095
Gene: VCP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35067988A>T , CM000671.2:g.35067988A>T GRCh38
NC_000009.11:g.35067985A>T , CM000671.1:g.35067985A>T GRCh37
NC_000009.10:g.35057985A>T NCBI36
NG_007887.1:g.9755T>A , LRG_657:g.9755T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000358901.11:c.205T>A MANE Select ENSP00000351777.6:p.Cys69Ser
ENST00000417448.2:c.70T>A ENSP00000399456.2:p.Cys24Ser
ENST00000448530.6:c.70T>A ENSP00000392088.2:p.Cys24Ser
ENST00000480327.2:n.477T>A
ENST00000676836.2:n.468T>A
ENST00000677257.1:c.199T>A ENSP00000504354.1:p.Cys67Ser
ENST00000678018.1:c.*176T>A ENSP00000503811.1:n.*176T>A
ENST00000678465.1:c.205T>A ENSP00000504259.1:p.Cys69Ser
ENST00000678650.1:c.70T>A ENSP00000503426.1:p.Cys24Ser
ENST00000679204.2:c.205T>A ENSP00000503131.2:p.Cys69Ser
ENST00000679449.1:c.224T>A
ENST00000679599.1:n.475T>A
ENST00000679647.1:c.205T>A ENSP00000506216.1:p.Cys69Ser
ENST00000679800.1:n.443T>A
ENST00000679862.1:c.70T>A ENSP00000504990.1:p.Cys24Ser
ENST00000679902.1:c.205T>A ENSP00000506338.1:p.Cys69Ser
ENST00000680079.1:c.*126T>A ENSP00000506523.1:n.*126T>A
ENST00000680731.1:c.70T>A ENSP00000505497.1:p.Cys24Ser
ENST00000680900.1:c.209T>A
ENST00000680916.1:c.205T>A ENSP00000505769.1:p.Cys69Ser
ENST00000681335.1:c.205T>A ENSP00000505230.1:p.Cys69Ser
ENST00000681386.1:c.70T>A ENSP00000505509.1:p.Cys24Ser
ENST00000681690.1:n.477T>A
ENST00000681845.1:c.371T>A
ENST00000358901.10:c.205T>A ENSP00000351777.6:p.Cys69Ser
ENST00000417448.1:c.70T>A ENSP00000399456.1:p.Cys24Ser
ENST00000448530.5:c.70T>A ENSP00000392088.1:p.Cys24Ser
ENST00000493886.5:n.401T>A
NM_007126.3:c.205T>A , LRG_657t1:c.205T>A NP_009057.1:p.Cys69Ser
NM_001354927.1:c.70T>A NP_001341856.1:p.Cys24Ser
NM_001354928.1:c.70T>A NP_001341857.1:p.Cys24Ser
NM_007126.4:c.205T>A NP_009057.1:p.Cys69Ser
NM_007126.5:c.205T>A MANE Select NP_009057.1:p.Cys69Ser
NM_001354927.2:c.70T>A NP_001341856.1:p.Cys24Ser
NM_001354928.2:c.70T>A NP_001341857.1:p.Cys24Ser