Canonical Allele Identifier: CA470165462

Gene: VCL

Linked Data

• ClinVar Variation Id: 1109053
• ClinVar RCV Id: RCV001434753
• dbSNP Id: rs372381809
• gnomAD v4: 10-74111965-C-A
• MyVariant Identifiers: chr10:g.75871723C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74111965C>A , CM000672.2:g.74111965C>A	GRCh38
NC_000010.10:g.75871723C>A , CM000672.1:g.75871723C>A	GRCh37
NC_000010.9:g.75541729C>A	NCBI36
NG_008868.1:g.118852C>A , LRG_383:g.118852C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2802C>A MANE Select	ENSP00000211998.5:p.Ala934=
ENST00000211998.8:c.2802C>A	ENSP00000211998.4:p.Ala934=
ENST00000372755.7:c.2746-2219C>A	ENSP00000361841.3:n.2746-2219C>A
ENST00000436396.1:c.1818C>A	ENSP00000415489.1:p.Ala606=
ENST00000623461.3:n.5549-2219C>A
ENST00000624354.3:c.*2557C>A	ENSP00000485551.1:n.*2557C>A
NM_003373.3:c.2746-2219C>A	NP_003364.1:n.2746-2219C>A
NM_014000.2:c.2802C>A , LRG_383t1:c.2802C>A	NP_054706.1:p.Ala934=
XM_005270142.1:c.2805C>A	XP_005270199.1:p.Ala935=
XM_005270143.1:c.2749-2219C>A	XP_005270200.1:n.2749-2219C>A
NM_003373.4:c.2746-2219C>A	NP_003364.1:n.2746-2219C>A
NM_014000.3:c.2802C>A MANE Select	NP_054706.1:p.Ala934=