Canonical Allele Identifier: CA1148076650
Gene: VANGL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425026G= , CM000663.2:g.160425026G= GRCh38
NC_000001.10:g.160394816G= , CM000663.1:g.160394816G= GRCh37
NC_000001.9:g.158661440G= NCBI36
NG_023420.1:g.29453G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-92G= ENSP00000512747.1:n.1450-92G=
ENST00000368061.3:c.1306-92G= MANE Select ENSP00000357040.2:n.1306-92G=
ENST00000368061.2:c.1306-92G= ENSP00000357040.2:n.1306-92G=
NM_020335.2:c.1306-92G= NP_065068.1:n.1306-92G=
XM_005245357.1:c.1306-92G= XP_005245414.1:n.1306-92G=
XM_011509804.1:c.1306-92G= XP_011508106.1:n.1306-92G=
NM_020335.3:c.1306-92G= MANE Select NP_065068.1:n.1306-92G=
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