Canonical Allele Identifier: CA929959921

Gene: VCL

Linked Data

• dbSNP Id: rs1839930503
• gnomAD v3: 10-74094192-G-A
• gnomAD v4: 10-74094192-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74094192G>A , CM000672.2:g.74094192G>A	GRCh38
NC_000010.10:g.75853950G>A , CM000672.1:g.75853950G>A	GRCh37
NC_000010.9:g.75523956G>A	NCBI36
NG_008868.1:g.101079G>A , LRG_383:g.101079G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000211998.10:c.1353-79G>A MANE Select	ENSP00000211998.5:n.1353-79G>A
ENST00000211998.8:c.1353-79G>A	ENSP00000211998.4:n.1353-79G>A
ENST00000372755.7:c.1353-79G>A	ENSP00000361841.3:n.1353-79G>A
ENST00000436396.1:c.369-79G>A	ENSP00000415489.1:n.369-79G>A
ENST00000478896.2:n.332-6862G>A
ENST00000623461.3:n.4156-79G>A
ENST00000624354.3:c.*1108-79G>A	ENSP00000485551.1:n.*1108-79G>A
NM_003373.3:c.1353-79G>A	NP_003364.1:n.1353-79G>A
NM_014000.2:c.1353-79G>A , LRG_383t1:c.1353-79G>A	NP_054706.1:n.1353-79G>A
XM_005270142.1:c.1356-79G>A	XP_005270199.1:n.1356-79G>A
XM_005270143.1:c.1356-79G>A	XP_005270200.1:n.1356-79G>A
NM_003373.4:c.1353-79G>A	NP_003364.1:n.1353-79G>A
NM_014000.3:c.1353-79G>A MANE Select	NP_054706.1:n.1353-79G>A