Canonical Allele Identifier: CA377277658

Gene: VCL

Linked Data

• dbSNP Id: rs1840044602
• MyVariant Identifiers: chr10:g.75860760A>G (hg19) ; chr10:g.74101002A>G (hg38)
• PubMed: PMID:25363768

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74101002A>G , CM000672.2:g.74101002A>G	GRCh38
NC_000010.10:g.75860760A>G , CM000672.1:g.75860760A>G	GRCh37
NC_000010.9:g.75530766A>G	NCBI36
NG_008868.1:g.107889A>G , LRG_383:g.107889A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1927A>G MANE Select	ENSP00000211998.5:p.Thr643Ala
ENST00000211998.8:c.1927A>G	ENSP00000211998.4:p.Thr643Ala
ENST00000372755.7:c.1927A>G	ENSP00000361841.3:p.Thr643Ala
ENST00000436396.1:c.943A>G	ENSP00000415489.1:p.Thr315Ala
ENST00000478896.2:n.332-52A>G
ENST00000623461.3:n.4730A>G
ENST00000624354.3:c.*1682A>G	ENSP00000485551.1:n.*1682A>G
NM_003373.3:c.1927A>G	NP_003364.1:p.Thr643Ala
NM_014000.2:c.1927A>G , LRG_383t1:c.1927A>G	NP_054706.1:p.Thr643Ala
XM_005270142.1:c.1930A>G	XP_005270199.1:p.Thr644Ala
XM_005270143.1:c.1930A>G	XP_005270200.1:p.Thr644Ala
NM_003373.4:c.1927A>G	NP_003364.1:p.Thr643Ala
NM_014000.3:c.1927A>G MANE Select	NP_054706.1:p.Thr643Ala