Canonical Allele Identifier: CA470171014

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842230A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082472A>C , CM000672.2:g.74082472A>C	GRCh38
NC_000010.10:g.75842230A>C , CM000672.1:g.75842230A>C	GRCh37
NC_000010.9:g.75512236A>C	NCBI36
NG_008868.1:g.89359A>C , LRG_383:g.89359A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.802A>C MANE Select	ENSP00000211998.5:p.Arg268=
ENST00000211998.8:c.802A>C	ENSP00000211998.4:p.Arg268=
ENST00000372755.7:c.802A>C	ENSP00000361841.3:p.Arg268=
ENST00000478896.2:n.332-18582A>C
ENST00000623461.3:n.3605A>C
ENST00000624354.3:c.*557A>C	ENSP00000485551.1:n.*557A>C
NM_003373.3:c.802A>C	NP_003364.1:p.Arg268=
NM_014000.2:c.802A>C , LRG_383t1:c.802A>C	NP_054706.1:p.Arg268=
XM_005270142.1:c.805A>C	XP_005270199.1:p.Arg269=
XM_005270143.1:c.805A>C	XP_005270200.1:p.Arg269=
XR_001747501.1:n.90-4745T>G
NM_003373.4:c.802A>C	NP_003364.1:p.Arg268=
NM_014000.3:c.802A>C MANE Select	NP_054706.1:p.Arg268=