Canonical Allele Identifier: CA377266726

Gene: VCL

Linked Data

• dbSNP Id: rs1591686988
• MyVariant Identifiers: chr10:g.75830815T>G (hg19) ; chr10:g.74071057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071057T>G , CM000672.2:g.74071057T>G	GRCh38
NC_000010.10:g.75830815T>G , CM000672.1:g.75830815T>G	GRCh37
NC_000010.9:g.75500821T>G	NCBI36
NG_008868.1:g.77944T>G , LRG_383:g.77944T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.473T>G MANE Select	ENSP00000211998.5:p.Val158Gly
ENST00000211998.8:c.473T>G	ENSP00000211998.4:p.Val158Gly
ENST00000372755.7:c.473T>G	ENSP00000361841.3:p.Val158Gly
ENST00000478896.2:n.331+27904T>G
ENST00000623461.3:n.431T>G
ENST00000624354.3:c.*228T>G	ENSP00000485551.1:n.*228T>G
NM_003373.3:c.473T>G	NP_003364.1:p.Val158Gly
NM_014000.2:c.473T>G , LRG_383t1:c.473T>G	NP_054706.1:p.Val158Gly
XM_005270142.1:c.473T>G	XP_005270199.1:p.Val158Gly
XM_005270143.1:c.473T>G	XP_005270200.1:p.Val158Gly
NM_003373.4:c.473T>G	NP_003364.1:p.Val158Gly
NM_014000.3:c.473T>G MANE Select	NP_054706.1:p.Val158Gly