Canonical Allele Identifier: CA2648683993
Gene: VANGL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425036del , CM000663.2:g.160425036del GRCh38
NC_000001.10:g.160394826del , CM000663.1:g.160394826del GRCh37
NC_000001.9:g.158661450del NCBI36
NG_023420.1:g.29463del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-82del ENSP00000512747.1:n.1450-82del
ENST00000368061.3:c.1306-82del MANE Select ENSP00000357040.2:n.1306-82del
ENST00000368061.2:c.1306-82del ENSP00000357040.2:n.1306-82del
NM_020335.2:c.1306-82del NP_065068.1:n.1306-82del
XM_005245357.1:c.1306-82del XP_005245414.1:n.1306-82del
XM_011509804.1:c.1306-82del XP_011508106.1:n.1306-82del
NM_020335.3:c.1306-82del MANE Select NP_065068.1:n.1306-82del