Canonical Allele Identifier: CA376174915

Gene: VIM VIM-AS1

Linked Data

• ClinVar Variation Id: 2872982
• ClinVar RCV Id: RCV003742422
• gnomAD v4: 10-17229504-C-G
• MyVariant Identifiers: chr10:g.17271503C>G (hg19) ; chr10:g.17229504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17229504C>G , CM000672.2:g.17229504C>G	GRCh38
NC_000010.10:g.17271503C>G , CM000672.1:g.17271503C>G	GRCh37
NC_000010.9:g.17311509C>G	NCBI36
NG_012413.1:g.6246C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544301.7:c.82C>G (VIM) MANE Select	ENSP00000446007.1:p.Arg28Gly
ENST00000224237.9:c.82C>G (VIM)	ENSP00000224237.5:p.Arg28Gly
ENST00000478317.5:n.495C>G (VIM)
ENST00000478746.1:n.391C>G (VIM)
ENST00000485947.1:n.214C>G (VIM)
ENST00000487938.5:c.82C>G (VIM)	ENSP00000435613.1:p.Arg28Gly
ENST00000497849.1:n.388C>G (VIM)
ENST00000544301.5:c.82C>G (VIM)	ENSP00000446007.1:p.Arg28Gly
NM_003380.3:c.82C>G (VIM)	NP_003371.2:p.Arg28Gly
NR_108061.1:n.482G>C (VIM-AS1)
XM_006717500.1:c.82C>G (VIM)	XP_006717563.1:p.Arg28Gly
XM_011519649.1:c.82C>G (VIM)	XP_011517951.1:p.Arg28Gly
NM_003380.4:c.82C>G (VIM)	NP_003371.2:p.Arg28Gly
XM_006717500.2:c.82C>G (VIM)	XP_006717563.1:p.Arg28Gly
NM_003380.5:c.82C>G (VIM) MANE Select	NP_003371.2:p.Arg28Gly