Canonical Allele Identifier: CA373293746

Gene: VCP

Linked Data

• MyVariant Identifiers: chr9:g.35067945A>G (hg19) ; chr9:g.35067948A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35067948A>G , CM000671.2:g.35067948A>G	GRCh38
NC_000009.11:g.35067945A>G , CM000671.1:g.35067945A>G	GRCh37
NC_000009.10:g.35057945A>G	NCBI36
NG_007887.1:g.9795T>C , LRG_657:g.9795T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358901.11:c.245T>C MANE Select	ENSP00000351777.6:p.Ile82Thr
ENST00000417448.2:c.110T>C	ENSP00000399456.2:p.Ile37Thr
ENST00000448530.6:c.110T>C	ENSP00000392088.2:p.Ile37Thr
ENST00000480327.2:n.517T>C
ENST00000676836.2:n.508T>C
ENST00000677257.1:c.239T>C	ENSP00000504354.1:p.Ile80Thr
ENST00000678018.1:c.*216T>C	ENSP00000503811.1:n.*216T>C
ENST00000678465.1:c.245T>C	ENSP00000504259.1:p.Ile82Thr
ENST00000678650.1:c.110T>C	ENSP00000503426.1:p.Ile37Thr
ENST00000679204.2:c.245T>C	ENSP00000503131.2:p.Ile82Thr
ENST00000679449.1:c.264T>C
ENST00000679599.1:n.515T>C
ENST00000679647.1:c.245T>C	ENSP00000506216.1:p.Ile82Thr
ENST00000679800.1:n.483T>C
ENST00000679862.1:c.110T>C	ENSP00000504990.1:p.Ile37Thr
ENST00000679902.1:c.245T>C	ENSP00000506338.1:p.Ile82Thr
ENST00000680079.1:c.*166T>C	ENSP00000506523.1:n.*166T>C
ENST00000680731.1:c.110T>C	ENSP00000505497.1:p.Ile37Thr
ENST00000680900.1:c.249T>C
ENST00000680916.1:c.245T>C	ENSP00000505769.1:p.Ile82Thr
ENST00000681335.1:c.245T>C	ENSP00000505230.1:p.Ile82Thr
ENST00000681386.1:c.110T>C	ENSP00000505509.1:p.Ile37Thr
ENST00000681690.1:n.517T>C
ENST00000681845.1:c.411T>C
ENST00000358901.10:c.245T>C	ENSP00000351777.6:p.Ile82Thr
ENST00000417448.1:c.110T>C	ENSP00000399456.1:p.Ile37Thr
ENST00000448530.5:c.110T>C	ENSP00000392088.1:p.Ile37Thr
ENST00000493886.5:n.441T>C
NM_007126.3:c.245T>C , LRG_657t1:c.245T>C	NP_009057.1:p.Ile82Thr
NM_001354927.1:c.110T>C	NP_001341856.1:p.Ile37Thr
NM_001354928.1:c.110T>C	NP_001341857.1:p.Ile37Thr
NM_007126.4:c.245T>C	NP_009057.1:p.Ile82Thr
NM_007126.5:c.245T>C MANE Select	NP_009057.1:p.Ile82Thr
NM_001354927.2:c.110T>C	NP_001341856.1:p.Ile37Thr
NM_001354928.2:c.110T>C	NP_001341857.1:p.Ile37Thr