Canonical Allele Identifier: CA333109

Gene: VCL

Linked Data

• ClinVar Variation Id: 137903
• ClinVar RCV Id: RCV000126294
• dbSNP Id: rs145537824
• ExAC: 10:75854010 G / A
• gnomAD v2: 10-75854010-G-A
• gnomAD v3: 10-74094252-G-A
• gnomAD v4: 10-74094252-G-A
• MyVariant Identifiers: chr10:g.75854010G>A (hg19) ; chr10:g.74094252G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094252G>A , CM000672.2:g.74094252G>A	GRCh38
NC_000010.10:g.75854010G>A , CM000672.1:g.75854010G>A	GRCh37
NC_000010.9:g.75524016G>A	NCBI36
NG_008868.1:g.101139G>A , LRG_383:g.101139G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.1353-19G>A MANE Select	ENSP00000211998.5:n.1353-19G>A
ENST00000211998.8:c.1353-19G>A	ENSP00000211998.4:n.1353-19G>A
ENST00000372755.7:c.1353-19G>A	ENSP00000361841.3:n.1353-19G>A
ENST00000436396.1:c.369-19G>A	ENSP00000415489.1:n.369-19G>A
ENST00000478896.2:n.332-6802G>A
ENST00000623461.3:n.4156-19G>A
ENST00000624354.3:c.*1108-19G>A	ENSP00000485551.1:n.*1108-19G>A
NM_003373.3:c.1353-19G>A	NP_003364.1:n.1353-19G>A
NM_014000.2:c.1353-19G>A , LRG_383t1:c.1353-19G>A	NP_054706.1:n.1353-19G>A
XM_005270142.1:c.1356-19G>A	XP_005270199.1:n.1356-19G>A
XM_005270143.1:c.1356-19G>A	XP_005270200.1:n.1356-19G>A
NM_003373.4:c.1353-19G>A	NP_003364.1:n.1353-19G>A
NM_014000.3:c.1353-19G>A MANE Select	NP_054706.1:n.1353-19G>A