Canonical Allele Identifier: CA2609715948

Gene: VCL

Linked Data

• gnomAD v4: 10-74094193-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094193C>G , CM000672.2:g.74094193C>G	GRCh38
NC_000010.10:g.75853951C>G , CM000672.1:g.75853951C>G	GRCh37
NC_000010.9:g.75523957C>G	NCBI36
NG_008868.1:g.101080C>G , LRG_383:g.101080C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-78C>G MANE Select	ENSP00000211998.5:n.1353-78C>G
ENST00000211998.8:c.1353-78C>G	ENSP00000211998.4:n.1353-78C>G
ENST00000372755.7:c.1353-78C>G	ENSP00000361841.3:n.1353-78C>G
ENST00000436396.1:c.369-78C>G	ENSP00000415489.1:n.369-78C>G
ENST00000478896.2:n.332-6861C>G
ENST00000623461.3:n.4156-78C>G
ENST00000624354.3:c.*1108-78C>G	ENSP00000485551.1:n.*1108-78C>G
NM_003373.3:c.1353-78C>G	NP_003364.1:n.1353-78C>G
NM_014000.2:c.1353-78C>G , LRG_383t1:c.1353-78C>G	NP_054706.1:n.1353-78C>G
XM_005270142.1:c.1356-78C>G	XP_005270199.1:n.1356-78C>G
XM_005270143.1:c.1356-78C>G	XP_005270200.1:n.1356-78C>G
NM_003373.4:c.1353-78C>G	NP_003364.1:n.1353-78C>G
NM_014000.3:c.1353-78C>G MANE Select	NP_054706.1:n.1353-78C>G