Canonical Allele Identifier: CA2574074965
Gene: VANGL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160425043A>T , CM000663.2:g.160425043A>T GRCh38
NC_000001.10:g.160394833A>T , CM000663.1:g.160394833A>T GRCh37
NC_000001.9:g.158661457A>T NCBI36
NG_023420.1:g.29470A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696602.1:c.1450-75A>T ENSP00000512747.1:n.1450-75A>T
ENST00000368061.3:c.1306-75A>T MANE Select ENSP00000357040.2:n.1306-75A>T
ENST00000368061.2:c.1306-75A>T ENSP00000357040.2:n.1306-75A>T
NM_020335.2:c.1306-75A>T NP_065068.1:n.1306-75A>T
XM_005245357.1:c.1306-75A>T XP_005245414.1:n.1306-75A>T
XM_011509804.1:c.1306-75A>T XP_011508106.1:n.1306-75A>T
NM_020335.3:c.1306-75A>T MANE Select NP_065068.1:n.1306-75A>T