Canonical Allele Identifier: CA594396788

Gene: VCL

Linked Data

• dbSNP Id: rs1455223111
• gnomAD v2: 10-75853988-A-C
• gnomAD v4: 10-74094230-A-C
• MyVariant Identifiers: chr10:g.75853988A>C (hg19) ; chr10:g.74094230A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094230A>C , CM000672.2:g.74094230A>C	GRCh38
NC_000010.10:g.75853988A>C , CM000672.1:g.75853988A>C	GRCh37
NC_000010.9:g.75523994A>C	NCBI36
NG_008868.1:g.101117A>C , LRG_383:g.101117A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-41A>C MANE Select	ENSP00000211998.5:n.1353-41A>C
ENST00000211998.8:c.1353-41A>C	ENSP00000211998.4:n.1353-41A>C
ENST00000372755.7:c.1353-41A>C	ENSP00000361841.3:n.1353-41A>C
ENST00000436396.1:c.369-41A>C	ENSP00000415489.1:n.369-41A>C
ENST00000478896.2:n.332-6824A>C
ENST00000623461.3:n.4156-41A>C
ENST00000624354.3:c.*1108-41A>C	ENSP00000485551.1:n.*1108-41A>C
NM_003373.3:c.1353-41A>C	NP_003364.1:n.1353-41A>C
NM_014000.2:c.1353-41A>C , LRG_383t1:c.1353-41A>C	NP_054706.1:n.1353-41A>C
XM_005270142.1:c.1356-41A>C	XP_005270199.1:n.1356-41A>C
XM_005270143.1:c.1356-41A>C	XP_005270200.1:n.1356-41A>C
NM_003373.4:c.1353-41A>C	NP_003364.1:n.1353-41A>C
NM_014000.3:c.1353-41A>C MANE Select	NP_054706.1:n.1353-41A>C