Canonical Allele Identifier: CA668315563

Gene: VCL

Linked Data

• dbSNP Id: rs1487176545
• gnomAD v3: 10-74119529-G-A
• gnomAD v4: 10-74119529-G-A
• MyVariant Identifiers: chr10:g.75879287G>A (hg19) ; chr10:g.74119529G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74119529G>A , CM000672.2:g.74119529G>A	GRCh38
NC_000010.10:g.75879287G>A , CM000672.1:g.75879287G>A	GRCh37
NC_000010.9:g.75549293G>A	NCBI36
NG_008868.1:g.126416G>A , LRG_383:g.126416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.*1360G>A MANE Select	ENSP00000211998.5:n.*1360G>A
ENST00000211998.8:c.*1360G>A	ENSP00000211998.4:n.*1360G>A
ENST00000372755.7:c.*1360G>A	ENSP00000361841.3:n.*1360G>A
ENST00000436396.1:c.3781G>A	ENSP00000415489.1:n.3781G>A
ENST00000623461.3:n.7364G>A
NM_003373.3:c.*1360G>A	NP_003364.1:n.*1360G>A
NM_014000.2:c.*1360G>A , LRG_383t1:c.*1360G>A	NP_054706.1:n.*1360G>A
XM_005270142.1:c.*1360G>A	XP_005270199.1:n.*1360G>A
XM_005270143.1:c.*1360G>A	XP_005270200.1:n.*1360G>A
NM_003373.4:c.*1360G>A	NP_003364.1:n.*1360G>A
NM_014000.3:c.*1360G>A MANE Select	NP_054706.1:n.*1360G>A