Canonical Allele Identifier: CA2574074966
Gene: VANGL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425053dup , CM000663.2:g.160425053dup GRCh38
NC_000001.10:g.160394843dup , CM000663.1:g.160394843dup GRCh37
NC_000001.9:g.158661467dup NCBI36
NG_023420.1:g.29480dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-65dup ENSP00000512747.1:n.1450-65dup
ENST00000368061.3:c.1306-65dup MANE Select ENSP00000357040.2:n.1306-65dup
ENST00000368061.2:c.1306-65dup ENSP00000357040.2:n.1306-65dup
NM_020335.2:c.1306-65dup NP_065068.1:n.1306-65dup
XM_005245357.1:c.1306-65dup XP_005245414.1:n.1306-65dup
XM_011509804.1:c.1306-65dup XP_011508106.1:n.1306-65dup
NM_020335.3:c.1306-65dup MANE Select NP_065068.1:n.1306-65dup