Canonical Allele Identifier: CA214748

Gene: VIM VIM-AS1

Linked Data

• ClinVar Variation Id: 12199
• ClinVar RCV Id: RCV000012983 ; RCV000056967
• dbSNP Id: rs121917775
• gnomAD v2: 10-17271872-G-A
• gnomAD v3: 10-17229873-G-A
• gnomAD v4: 10-17229873-G-A
• MyVariant Identifiers: chr10:g.17271872G>A (hg19) ; chr10:g.17229873G>A (hg38)
• PubMed: PMID:19126778

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17229873G>A , CM000672.2:g.17229873G>A	GRCh38
NC_000010.10:g.17271872G>A , CM000672.1:g.17271872G>A	GRCh37
NC_000010.9:g.17311878G>A	NCBI36
NG_012413.1:g.6615G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000544301.7:c.451G>A (VIM) MANE Select	ENSP00000446007.1:p.Glu151Lys
ENST00000224237.9:c.451G>A (VIM)	ENSP00000224237.5:p.Glu151Lys
ENST00000478317.5:n.864G>A (VIM)
ENST00000485947.1:n.583G>A (VIM)
ENST00000487938.5:c.451G>A (VIM)	ENSP00000435613.1:p.Glu151Lys
ENST00000544301.5:c.451G>A (VIM)	ENSP00000446007.1:p.Glu151Lys
NM_003380.3:c.451G>A (VIM)	NP_003371.2:p.Glu151Lys
NR_108061.1:n.113C>T (VIM-AS1)
XM_006717500.1:c.451G>A (VIM)	XP_006717563.1:p.Glu151Lys
XM_011519649.1:c.451G>A (VIM)	XP_011517951.1:p.Glu151Lys
NM_003380.4:c.451G>A (VIM)	NP_003371.2:p.Glu151Lys
XM_006717500.2:c.451G>A (VIM)	XP_006717563.1:p.Glu151Lys
NM_003380.5:c.451G>A (VIM) MANE Select	NP_003371.2:p.Glu151Lys