Canonical Allele Identifier: CA377266854

Gene: VCL

Linked Data

• gnomAD v4: 10-74071077-G-C
• MyVariant Identifiers: chr10:g.75830835G>C (hg19) ; chr10:g.74071077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74071077G>C , CM000672.2:g.74071077G>C	GRCh38
NC_000010.10:g.75830835G>C , CM000672.1:g.75830835G>C	GRCh37
NC_000010.9:g.75500841G>C	NCBI36
NG_008868.1:g.77964G>C , LRG_383:g.77964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.493G>C MANE Select	ENSP00000211998.5:p.Gly165Arg
ENST00000211998.8:c.493G>C	ENSP00000211998.4:p.Gly165Arg
ENST00000372755.7:c.493G>C	ENSP00000361841.3:p.Gly165Arg
ENST00000478896.2:n.331+27924G>C
ENST00000623461.3:n.451G>C
ENST00000624354.3:c.*248G>C	ENSP00000485551.1:n.*248G>C
NM_003373.3:c.493G>C	NP_003364.1:p.Gly165Arg
NM_014000.2:c.493G>C , LRG_383t1:c.493G>C	NP_054706.1:p.Gly165Arg
XM_005270142.1:c.493G>C	XP_005270199.1:p.Gly165Arg
XM_005270143.1:c.493G>C	XP_005270200.1:p.Gly165Arg
NM_003373.4:c.493G>C	NP_003364.1:p.Gly165Arg
NM_014000.3:c.493G>C MANE Select	NP_054706.1:p.Gly165Arg