Canonical Allele Identifier: CA5426364

Gene: VIM VIM-AS1

Linked Data

• ClinVar Variation Id: 541104
• ClinVar RCV Id: RCV000651306
• dbSNP Id: rs773938980
• ExAC: 10:17271588 C / A
• gnomAD v2: 10-17271588-C-A
• gnomAD v3: 10-17229589-C-A
• gnomAD v4: 10-17229589-C-A
• MyVariant Identifiers: chr10:g.17271588C>A (hg19) ; chr10:g.17229589C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17229589C>A , CM000672.2:g.17229589C>A	GRCh38
NC_000010.10:g.17271588C>A , CM000672.1:g.17271588C>A	GRCh37
NC_000010.9:g.17311594C>A	NCBI36
NG_012413.1:g.6331C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000544301.7:c.167C>A (VIM) MANE Select	ENSP00000446007.1:p.Ser56Tyr
ENST00000224237.9:c.167C>A (VIM)	ENSP00000224237.5:p.Ser56Tyr
ENST00000478317.5:n.580C>A (VIM)
ENST00000478746.1:n.476C>A (VIM)
ENST00000485947.1:n.299C>A (VIM)
ENST00000487938.5:c.167C>A (VIM)	ENSP00000435613.1:p.Ser56Tyr
ENST00000497849.1:n.473C>A (VIM)
ENST00000544301.5:c.167C>A (VIM)	ENSP00000446007.1:p.Ser56Tyr
NM_003380.3:c.167C>A (VIM)	NP_003371.2:p.Ser56Tyr
NR_108061.1:n.397G>T (VIM-AS1)
XM_006717500.1:c.167C>A (VIM)	XP_006717563.1:p.Ser56Tyr
XM_011519649.1:c.167C>A (VIM)	XP_011517951.1:p.Ser56Tyr
NM_003380.4:c.167C>A (VIM)	NP_003371.2:p.Ser56Tyr
XM_006717500.2:c.167C>A (VIM)	XP_006717563.1:p.Ser56Tyr
NM_003380.5:c.167C>A (VIM) MANE Select	NP_003371.2:p.Ser56Tyr