Canonical Allele Identifier: CA377266817

Gene: VCL

Linked Data

• ClinVar Variation Id: 1063922
• ClinVar RCV Id: RCV001373815 ; RCV004037586
• dbSNP Id: rs2136272931
• gnomAD v4: 10-74071071-A-G
• MyVariant Identifiers: chr10:g.75830829A>G (hg19) ; chr10:g.74071071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071071A>G , CM000672.2:g.74071071A>G	GRCh38
NC_000010.10:g.75830829A>G , CM000672.1:g.75830829A>G	GRCh37
NC_000010.9:g.75500835A>G	NCBI36
NG_008868.1:g.77958A>G , LRG_383:g.77958A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.487A>G MANE Select	ENSP00000211998.5:p.Asn163Asp
ENST00000211998.8:c.487A>G	ENSP00000211998.4:p.Asn163Asp
ENST00000372755.7:c.487A>G	ENSP00000361841.3:p.Asn163Asp
ENST00000478896.2:n.331+27918A>G
ENST00000623461.3:n.445A>G
ENST00000624354.3:c.*242A>G	ENSP00000485551.1:n.*242A>G
NM_003373.3:c.487A>G	NP_003364.1:p.Asn163Asp
NM_014000.2:c.487A>G , LRG_383t1:c.487A>G	NP_054706.1:p.Asn163Asp
XM_005270142.1:c.487A>G	XP_005270199.1:p.Asn163Asp
XM_005270143.1:c.487A>G	XP_005270200.1:p.Asn163Asp
NM_003373.4:c.487A>G	NP_003364.1:p.Asn163Asp
NM_014000.3:c.487A>G MANE Select	NP_054706.1:p.Asn163Asp