Canonical Allele Identifier: CA1145473912
Gene: VANGL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425058G= , CM000663.2:g.160425058G= GRCh38
NC_000001.10:g.160394848G= , CM000663.1:g.160394848G= GRCh37
NC_000001.9:g.158661472G= NCBI36
NG_023420.1:g.29485G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-60G= ENSP00000512747.1:n.1450-60G=
ENST00000368061.3:c.1306-60G= MANE Select ENSP00000357040.2:n.1306-60G=
ENST00000368061.2:c.1306-60G= ENSP00000357040.2:n.1306-60G=
NM_020335.2:c.1306-60G= NP_065068.1:n.1306-60G=
XM_005245357.1:c.1306-60G= XP_005245414.1:n.1306-60G=
XM_011509804.1:c.1306-60G= XP_011508106.1:n.1306-60G=
NM_020335.3:c.1306-60G= MANE Select NP_065068.1:n.1306-60G=