Canonical Allele Identifier: CA668301120

Gene: VCL

Linked Data

• dbSNP Id: rs1478746384
• MyVariant Identifiers: chr10:g.75853944C>T (hg19) ; chr10:g.74094186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094186C>T , CM000672.2:g.74094186C>T	GRCh38
NC_000010.10:g.75853944C>T , CM000672.1:g.75853944C>T	GRCh37
NC_000010.9:g.75523950C>T	NCBI36
NG_008868.1:g.101073C>T , LRG_383:g.101073C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-85C>T MANE Select	ENSP00000211998.5:n.1353-85C>T
ENST00000211998.8:c.1353-85C>T	ENSP00000211998.4:n.1353-85C>T
ENST00000372755.7:c.1353-85C>T	ENSP00000361841.3:n.1353-85C>T
ENST00000436396.1:c.369-85C>T	ENSP00000415489.1:n.369-85C>T
ENST00000478896.2:n.332-6868C>T
ENST00000623461.3:n.4156-85C>T
ENST00000624354.3:c.*1108-85C>T	ENSP00000485551.1:n.*1108-85C>T
NM_003373.3:c.1353-85C>T	NP_003364.1:n.1353-85C>T
NM_014000.2:c.1353-85C>T , LRG_383t1:c.1353-85C>T	NP_054706.1:n.1353-85C>T
XM_005270142.1:c.1356-85C>T	XP_005270199.1:n.1356-85C>T
XM_005270143.1:c.1356-85C>T	XP_005270200.1:n.1356-85C>T
NM_003373.4:c.1353-85C>T	NP_003364.1:n.1353-85C>T
NM_014000.3:c.1353-85C>T MANE Select	NP_054706.1:n.1353-85C>T