Canonical Allele Identifier: CA192695224

Gene: VCP

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35056077A>G , CM000671.2:g.35056077A>G	GRCh38
NC_000009.11:g.35056074A>G , CM000671.1:g.35056074A>G	GRCh37
NC_000009.10:g.35046074A>G	NCBI36
NG_007887.1:g.21666T>C , LRG_657:g.21666T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_007126.5:c.*1040T>C MANE Select	NP_009057.1:n.*1040T>C
ENST00000358901.11:c.*1040T>C MANE Select	ENSP00000351777.6:n.*1040T>C
NM_001354927.1:c.*1040T>C	NP_001341856.1:n.*1040T>C
NM_001354927.2:c.*1040T>C	NP_001341856.1:n.*1040T>C
NM_001354928.1:c.*1040T>C	NP_001341857.1:n.*1040T>C
NM_001354928.2:c.*1040T>C	NP_001341857.1:n.*1040T>C
NM_007126.3:c.*1040T>C , LRG_657t1:c.*1040T>C	NP_009057.1:n.*1040T>C
NM_007126.4:c.*1040T>C	NP_009057.1:n.*1040T>C
ENST00000358901.10:c.*1040T>C	ENSP00000351777.6:n.*1040T>C
ENST00000448530.6:c.*1040T>C	ENSP00000392088.2:n.*1040T>C
ENST00000677257.1:c.*1040T>C	ENSP00000504354.1:n.*1040T>C
ENST00000678018.1:c.*3432T>C	ENSP00000503811.1:n.*3432T>C
ENST00000678465.1:c.*2473T>C	ENSP00000504259.1:n.*2473T>C
ENST00000678650.1:c.*1040T>C	ENSP00000503426.1:n.*1040T>C
ENST00000679800.1:n.3860T>C
ENST00000679902.1:c.*1295T>C	ENSP00000506338.1:n.*1295T>C
ENST00000681537.1:c.1290T>C	ENSP00000505847.1:n.1290T>C