Canonical Allele Identifier: CA2745158504
Gene: VANGL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115683846_115683847dup , CM000663.2:g.115683846_115683847dup GRCh38
NC_000001.10:g.116226467_116226468dup , CM000663.1:g.116226467_116226468dup GRCh37
NC_000001.9:g.116027990_116027991dup NCBI36
NG_016548.1:g.46894_46895dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355485.7:c.947-98_947-97dup MANE Select ENSP00000347672.2:n.947-98_947-97dup
ENST00000310260.7:c.947-98_947-97dup ENSP00000310800.3:n.947-98_947-97dup
ENST00000355485.6:c.947-98_947-97dup ENSP00000347672.2:n.947-98_947-97dup
ENST00000369509.1:c.947-98_947-97dup ENSP00000358522.1:n.947-98_947-97dup
ENST00000369510.8:c.941-98_941-97dup ENSP00000358523.3:n.941-98_941-97dup
ENST00000474344.1:n.329-98_329-97dup
ENST00000478369.5:n.231-98_231-97dup
NM_001172411.1:c.941-98_941-97dup NP_001165882.1:n.941-98_941-97dup
NM_001172412.1:c.947-98_947-97dup NP_001165883.1:n.947-98_947-97dup
NM_138959.2:c.947-98_947-97dup NP_620409.1:n.947-98_947-97dup
NM_138959.3:c.947-98_947-97dup MANE Select NP_620409.1:n.947-98_947-97dup
NM_001172411.2:c.941-98_941-97dup NP_001165882.1:n.941-98_941-97dup
NM_001172412.2:c.947-98_947-97dup NP_001165883.1:n.947-98_947-97dup