Canonical Allele Identifier: CA1202313682
Gene: VANGL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425028C= , CM000663.2:g.160425028C= GRCh38
NC_000001.10:g.160394818C= , CM000663.1:g.160394818C= GRCh37
NC_000001.9:g.158661442C= NCBI36
NG_023420.1:g.29455C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-90C= ENSP00000512747.1:n.1450-90C=
ENST00000368061.3:c.1306-90C= MANE Select ENSP00000357040.2:n.1306-90C=
ENST00000368061.2:c.1306-90C= ENSP00000357040.2:n.1306-90C=
NM_020335.2:c.1306-90C= NP_065068.1:n.1306-90C=
XM_005245357.1:c.1306-90C= XP_005245414.1:n.1306-90C=
XM_011509804.1:c.1306-90C= XP_011508106.1:n.1306-90C=
NM_020335.3:c.1306-90C= MANE Select NP_065068.1:n.1306-90C=