Canonical Allele Identifier: CA1190705807
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115683834_115683835delinsTG , CM000663.2:g.115683834_115683835delinsTG GRCh38
NC_000001.10:g.116226455_116226456delinsTG , CM000663.1:g.116226455_116226456delinsTG GRCh37
NC_000001.9:g.116027978_116027979delinsTG NCBI36
NG_016548.1:g.46882_46883delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355485.7:c.947-110_947-109delinsTG MANE Select ENSP00000347672.2:n.947-110_947-109delinsTG
ENST00000310260.7:c.947-110_947-109delinsTG ENSP00000310800.3:n.947-110_947-109delinsTG
ENST00000355485.6:c.947-110_947-109delinsTG ENSP00000347672.2:n.947-110_947-109delinsTG
ENST00000369509.1:c.947-110_947-109delinsTG ENSP00000358522.1:n.947-110_947-109delinsTG
ENST00000369510.8:c.941-110_941-109delinsTG ENSP00000358523.3:n.941-110_941-109delinsTG
ENST00000474344.1:n.329-110_329-109delinsTG
ENST00000478369.5:n.231-110_231-109delinsTG
NM_001172411.1:c.941-110_941-109delinsTG NP_001165882.1:n.941-110_941-109delinsTG
NM_001172412.1:c.947-110_947-109delinsTG NP_001165883.1:n.947-110_947-109delinsTG
NM_138959.2:c.947-110_947-109delinsTG NP_620409.1:n.947-110_947-109delinsTG
NM_138959.3:c.947-110_947-109delinsTG MANE Select NP_620409.1:n.947-110_947-109delinsTG
NM_001172411.2:c.941-110_941-109delinsTG NP_001165882.1:n.941-110_941-109delinsTG
NM_001172412.2:c.947-110_947-109delinsTG NP_001165883.1:n.947-110_947-109delinsTG