Canonical Allele Identifier: CA1148236587
Gene: VANGL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425051A= , CM000663.2:g.160425051A= GRCh38
NC_000001.10:g.160394841A= , CM000663.1:g.160394841A= GRCh37
NC_000001.9:g.158661465A= NCBI36
NG_023420.1:g.29478A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696602.1:c.1450-67A= ENSP00000512747.1:n.1450-67A=
ENST00000368061.3:c.1306-67A= MANE Select ENSP00000357040.2:n.1306-67A=
ENST00000368061.2:c.1306-67A= ENSP00000357040.2:n.1306-67A=
NM_020335.2:c.1306-67A= NP_065068.1:n.1306-67A=
XM_005245357.1:c.1306-67A= XP_005245414.1:n.1306-67A=
XM_011509804.1:c.1306-67A= XP_011508106.1:n.1306-67A=
NM_020335.3:c.1306-67A= MANE Select NP_065068.1:n.1306-67A=