Canonical Allele Identifier: CA2588861823

Gene: VCL

Linked Data

• dbSNP Id: rs2136280171
• gnomAD v3: 10-74082357-T-A
• gnomAD v4: 10-74082357-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082357T>A , CM000672.2:g.74082357T>A	GRCh38
NC_000010.10:g.75842115T>A , CM000672.1:g.75842115T>A	GRCh37
NC_000010.9:g.75512121T>A	NCBI36
NG_008868.1:g.89244T>A , LRG_383:g.89244T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.784-97T>A MANE Select	ENSP00000211998.5:n.784-97T>A
ENST00000211998.8:c.784-97T>A	ENSP00000211998.4:n.784-97T>A
ENST00000372755.7:c.784-97T>A	ENSP00000361841.3:n.784-97T>A
ENST00000478896.2:n.332-18697T>A
ENST00000623461.3:n.3587-97T>A
ENST00000624354.3:c.*539-97T>A	ENSP00000485551.1:n.*539-97T>A
NM_003373.3:c.784-97T>A	NP_003364.1:n.784-97T>A
NM_014000.2:c.784-97T>A , LRG_383t1:c.784-97T>A	NP_054706.1:n.784-97T>A
XM_005270142.1:c.784-94T>A	XP_005270199.1:n.784-94T>A
XM_005270143.1:c.784-94T>A	XP_005270200.1:n.784-94T>A
XR_001747501.1:n.90-4630A>T
NM_003373.4:c.784-97T>A	NP_003364.1:n.784-97T>A
NM_014000.3:c.784-97T>A MANE Select	NP_054706.1:n.784-97T>A