Canonical Allele Identifier: CA1144006544
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115683915A= , CM000663.2:g.115683915A= GRCh38
NC_000001.10:g.116226536A= , CM000663.1:g.116226536A= GRCh37
NC_000001.9:g.116028059A= NCBI36
NG_016548.1:g.46963A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355485.7:c.947-29A= MANE Select ENSP00000347672.2:n.947-29A=
ENST00000310260.7:c.947-29A= ENSP00000310800.3:n.947-29A=
ENST00000355485.6:c.947-29A= ENSP00000347672.2:n.947-29A=
ENST00000369509.1:c.947-29A= ENSP00000358522.1:n.947-29A=
ENST00000369510.8:c.941-29A= ENSP00000358523.3:n.941-29A=
ENST00000474344.1:n.329-29A=
ENST00000478369.5:n.231-29A=
NM_001172411.1:c.941-29A= NP_001165882.1:n.941-29A=
NM_001172412.1:c.947-29A= NP_001165883.1:n.947-29A=
NM_138959.2:c.947-29A= NP_620409.1:n.947-29A=
NM_138959.3:c.947-29A= MANE Select NP_620409.1:n.947-29A=
NM_001172411.2:c.941-29A= NP_001165882.1:n.941-29A=
NM_001172412.2:c.947-29A= NP_001165883.1:n.947-29A=