Canonical Allele Identifier: CA377269419

Gene: VCL

Linked Data

• MyVariant Identifiers: chr10:g.75842218G>C (hg19) ; chr10:g.74082460G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74082460G>C , CM000672.2:g.74082460G>C	GRCh38
NC_000010.10:g.75842218G>C , CM000672.1:g.75842218G>C	GRCh37
NC_000010.9:g.75512224G>C	NCBI36
NG_008868.1:g.89347G>C , LRG_383:g.89347G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.790G>C MANE Select	ENSP00000211998.5:p.Glu264Gln
ENST00000211998.8:c.790G>C	ENSP00000211998.4:p.Glu264Gln
ENST00000372755.7:c.790G>C	ENSP00000361841.3:p.Glu264Gln
ENST00000478896.2:n.332-18594G>C
ENST00000623461.3:n.3593G>C
ENST00000624354.3:c.*545G>C	ENSP00000485551.1:n.*545G>C
NM_003373.3:c.790G>C	NP_003364.1:p.Glu264Gln
NM_014000.2:c.790G>C , LRG_383t1:c.790G>C	NP_054706.1:p.Glu264Gln
XM_005270142.1:c.793G>C	XP_005270199.1:p.Glu265Gln
XM_005270143.1:c.793G>C	XP_005270200.1:p.Glu265Gln
XR_001747501.1:n.90-4733C>G
NM_003373.4:c.790G>C	NP_003364.1:p.Glu264Gln
NM_014000.3:c.790G>C MANE Select	NP_054706.1:p.Glu264Gln