Canonical Allele Identifier: CA1006076560

Gene: VANGL1

Linked Data

• dbSNP Id: rs1653484472
• gnomAD v3: 1-115683831-G-A
• gnomAD v4: 1-115683831-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115683831G>A , CM000663.2:g.115683831G>A	GRCh38
NC_000001.10:g.116226452G>A , CM000663.1:g.116226452G>A	GRCh37
NC_000001.9:g.116027975G>A	NCBI36
NG_016548.1:g.46879G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355485.7:c.947-113G>A MANE Select	ENSP00000347672.2:n.947-113G>A
ENST00000310260.7:c.947-113G>A	ENSP00000310800.3:n.947-113G>A
ENST00000355485.6:c.947-113G>A	ENSP00000347672.2:n.947-113G>A
ENST00000369509.1:c.947-113G>A	ENSP00000358522.1:n.947-113G>A
ENST00000369510.8:c.941-113G>A	ENSP00000358523.3:n.941-113G>A
ENST00000474344.1:n.329-113G>A
ENST00000478369.5:n.231-113G>A
NM_001172411.1:c.941-113G>A	NP_001165882.1:n.941-113G>A
NM_001172412.1:c.947-113G>A	NP_001165883.1:n.947-113G>A
NM_138959.2:c.947-113G>A	NP_620409.1:n.947-113G>A
NM_138959.3:c.947-113G>A MANE Select	NP_620409.1:n.947-113G>A
NM_001172411.2:c.941-113G>A	NP_001165882.1:n.941-113G>A
NM_001172412.2:c.947-113G>A	NP_001165883.1:n.947-113G>A