Canonical Allele Identifier: CA1202313691
Gene: VANGL2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425052C= , CM000663.2:g.160425052C= GRCh38
NC_000001.10:g.160394842C= , CM000663.1:g.160394842C= GRCh37
NC_000001.9:g.158661466C= NCBI36
NG_023420.1:g.29479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-66C= ENSP00000512747.1:n.1450-66C=
ENST00000368061.3:c.1306-66C= MANE Select ENSP00000357040.2:n.1306-66C=
ENST00000368061.2:c.1306-66C= ENSP00000357040.2:n.1306-66C=
NM_020335.2:c.1306-66C= NP_065068.1:n.1306-66C=
XM_005245357.1:c.1306-66C= XP_005245414.1:n.1306-66C=
XM_011509804.1:c.1306-66C= XP_011508106.1:n.1306-66C=
NM_020335.3:c.1306-66C= MANE Select NP_065068.1:n.1306-66C=
Search 100 bp 5'
Search 100 bp 3'