Canonical Allele Identifier: CA5562765

Gene: VCL

Linked Data

• dbSNP Id: rs776290040
• ExAC: 10:75830711 A / G
• gnomAD v2: 10-75830711-A-G
• gnomAD v4: 10-74070953-A-G
• MyVariant Identifiers: chr10:g.75830711A>G (hg19) ; chr10:g.74070953A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74070953A>G , CM000672.2:g.74070953A>G	GRCh38
NC_000010.10:g.75830711A>G , CM000672.1:g.75830711A>G	GRCh37
NC_000010.9:g.75500717A>G	NCBI36
NG_008868.1:g.77840A>G , LRG_383:g.77840A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000211998.10:c.391-22A>G MANE Select	ENSP00000211998.5:n.391-22A>G
ENST00000211998.8:c.391-22A>G	ENSP00000211998.4:n.391-22A>G
ENST00000372755.7:c.391-22A>G	ENSP00000361841.3:n.391-22A>G
ENST00000478896.2:n.331+27800A>G
ENST00000623461.3:n.349-22A>G
ENST00000624354.3:c.*146-22A>G	ENSP00000485551.1:n.*146-22A>G
NM_003373.3:c.391-22A>G	NP_003364.1:n.391-22A>G
NM_014000.2:c.391-22A>G , LRG_383t1:c.391-22A>G	NP_054706.1:n.391-22A>G
XM_005270142.1:c.391-22A>G	XP_005270199.1:n.391-22A>G
XM_005270143.1:c.391-22A>G	XP_005270200.1:n.391-22A>G
NM_003373.4:c.391-22A>G	NP_003364.1:n.391-22A>G
NM_014000.3:c.391-22A>G MANE Select	NP_054706.1:n.391-22A>G