Canonical Allele Identifier: CA1190705860
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115683971C= , CM000663.2:g.115683971C= GRCh38
NC_000001.10:g.116226592C= , CM000663.1:g.116226592C= GRCh37
NC_000001.9:g.116028115C= NCBI36
NG_016548.1:g.47019C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355485.7:c.974C= MANE Select ENSP00000347672.2:p.Ser325=
ENST00000310260.7:c.974C= ENSP00000310800.3:p.Ser325=
ENST00000355485.6:c.974C= ENSP00000347672.2:p.Ser325=
ENST00000369509.1:c.974C= ENSP00000358522.1:p.Ser325=
ENST00000369510.8:c.968C= ENSP00000358523.3:p.Ser323=
ENST00000474344.1:n.356C=
ENST00000478369.5:n.258C=
NM_001172411.1:c.968C= NP_001165882.1:p.Ser323=
NM_001172412.1:c.974C= NP_001165883.1:p.Ser325=
NM_138959.2:c.974C= NP_620409.1:p.Ser325=
NM_138959.3:c.974C= MANE Select NP_620409.1:p.Ser325=
NM_001172411.2:c.968C= NP_001165882.1:p.Ser323=
NM_001172412.2:c.974C= NP_001165883.1:p.Ser325=