Canonical Allele Identifier: CA1202313696
Gene: VANGL2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425061T= , CM000663.2:g.160425061T= GRCh38
NC_000001.10:g.160394851T= , CM000663.1:g.160394851T= GRCh37
NC_000001.9:g.158661475T= NCBI36
NG_023420.1:g.29488T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696602.1:c.1450-57T= ENSP00000512747.1:n.1450-57T=
ENST00000368061.3:c.1306-57T= MANE Select ENSP00000357040.2:n.1306-57T=
ENST00000368061.2:c.1306-57T= ENSP00000357040.2:n.1306-57T=
NM_020335.2:c.1306-57T= NP_065068.1:n.1306-57T=
XM_005245357.1:c.1306-57T= XP_005245414.1:n.1306-57T=
XM_011509804.1:c.1306-57T= XP_011508106.1:n.1306-57T=
NM_020335.3:c.1306-57T= MANE Select NP_065068.1:n.1306-57T=
Search 100 bp 5'
Search 100 bp 3'