Canonical Allele Identifier: CA341764663
Gene: VANGL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115683992C>G , CM000663.2:g.115683992C>G GRCh38
NC_000001.10:g.116226613C>G , CM000663.1:g.116226613C>G GRCh37
NC_000001.9:g.116028136C>G NCBI36
NG_016548.1:g.47040C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000355485.7:c.995C>G MANE Select ENSP00000347672.2:p.Ala332Gly
ENST00000310260.7:c.995C>G ENSP00000310800.3:p.Ala332Gly
ENST00000355485.6:c.995C>G ENSP00000347672.2:p.Ala332Gly
ENST00000369509.1:c.995C>G ENSP00000358522.1:p.Ala332Gly
ENST00000369510.8:c.989C>G ENSP00000358523.3:p.Ala330Gly
ENST00000474344.1:n.377C>G
ENST00000478369.5:n.279C>G
NM_001172411.1:c.989C>G NP_001165882.1:p.Ala330Gly
NM_001172412.1:c.995C>G NP_001165883.1:p.Ala332Gly
NM_138959.2:c.995C>G NP_620409.1:p.Ala332Gly
NM_138959.3:c.995C>G MANE Select NP_620409.1:p.Ala332Gly
NM_001172411.2:c.989C>G NP_001165882.1:p.Ala330Gly
NM_001172412.2:c.995C>G NP_001165883.1:p.Ala332Gly