Canonical Allele Identifier: CA2746346776
Gene: VANGL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425033T>G , CM000663.2:g.160425033T>G GRCh38
NC_000001.10:g.160394823T>G , CM000663.1:g.160394823T>G GRCh37
NC_000001.9:g.158661447T>G NCBI36
NG_023420.1:g.29460T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-85T>G ENSP00000512747.1:n.1450-85T>G
ENST00000368061.3:c.1306-85T>G MANE Select ENSP00000357040.2:n.1306-85T>G
ENST00000368061.2:c.1306-85T>G ENSP00000357040.2:n.1306-85T>G
NM_020335.2:c.1306-85T>G NP_065068.1:n.1306-85T>G
XM_005245357.1:c.1306-85T>G XP_005245414.1:n.1306-85T>G
XM_011509804.1:c.1306-85T>G XP_011508106.1:n.1306-85T>G
NM_020335.3:c.1306-85T>G MANE Select NP_065068.1:n.1306-85T>G