Canonical Allele Identifier: CA594389157

Gene: VCL

Linked Data

• dbSNP Id: rs1157244001
• gnomAD v2: 10-75866961-C-G
• gnomAD v4: 10-74107203-C-G
• MyVariant Identifiers: chr10:g.75866961C>G (hg19) ; chr10:g.74107203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74107203C>G , CM000672.2:g.74107203C>G	GRCh38
NC_000010.10:g.75866961C>G , CM000672.1:g.75866961C>G	GRCh37
NC_000010.9:g.75536967C>G	NCBI36
NG_008868.1:g.114090C>G , LRG_383:g.114090C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.2435-27C>G MANE Select	ENSP00000211998.5:n.2435-27C>G
ENST00000211998.8:c.2435-27C>G	ENSP00000211998.4:n.2435-27C>G
ENST00000372755.7:c.2435-27C>G	ENSP00000361841.3:n.2435-27C>G
ENST00000436396.1:c.1451-27C>G	ENSP00000415489.1:n.1451-27C>G
ENST00000472585.1:n.427-27C>G
ENST00000623461.3:n.5238-27C>G
ENST00000624354.3:c.*2190-27C>G	ENSP00000485551.1:n.*2190-27C>G
NM_003373.3:c.2435-27C>G	NP_003364.1:n.2435-27C>G
NM_014000.2:c.2435-27C>G , LRG_383t1:c.2435-27C>G	NP_054706.1:n.2435-27C>G
XM_005270142.1:c.2438-27C>G	XP_005270199.1:n.2438-27C>G
XM_005270143.1:c.2438-27C>G	XP_005270200.1:n.2438-27C>G
NM_003373.4:c.2435-27C>G	NP_003364.1:n.2435-27C>G
NM_014000.3:c.2435-27C>G MANE Select	NP_054706.1:n.2435-27C>G