Canonical Allele Identifier: CA377269738

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842278C>G (hg19) ; chr10:g.74082520C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082520C>G , CM000672.2:g.74082520C>G	GRCh38
NC_000010.10:g.75842278C>G , CM000672.1:g.75842278C>G	GRCh37
NC_000010.9:g.75512284C>G	NCBI36
NG_008868.1:g.89407C>G , LRG_383:g.89407C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.850C>G MANE Select	ENSP00000211998.5:p.Leu284Val
ENST00000211998.8:c.850C>G	ENSP00000211998.4:p.Leu284Val
ENST00000372755.7:c.850C>G	ENSP00000361841.3:p.Leu284Val
ENST00000478896.2:n.332-18534C>G
ENST00000623461.3:n.3653C>G
ENST00000624354.3:c.*605C>G	ENSP00000485551.1:n.*605C>G
NM_003373.3:c.850C>G	NP_003364.1:p.Leu284Val
NM_014000.2:c.850C>G , LRG_383t1:c.850C>G	NP_054706.1:p.Leu284Val
XM_005270142.1:c.853C>G	XP_005270199.1:p.Leu285Val
XM_005270143.1:c.853C>G	XP_005270200.1:p.Leu285Val
XR_001747501.1:n.90-4793G>C
NM_003373.4:c.850C>G	NP_003364.1:p.Leu284Val
NM_014000.3:c.850C>G MANE Select	NP_054706.1:p.Leu284Val