Canonical Allele Identifier: CA1190705833

Gene: VANGL1

Linked Data

• dbSNP Id: rs1653488330

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115683911_115683912insCTTT , CM000663.2:g.115683911_115683912insCTTT	GRCh38
NC_000001.10:g.116226532_116226533insCTTT , CM000663.1:g.116226532_116226533insCTTT	GRCh37
NC_000001.9:g.116028055_116028056insCTTT	NCBI36
NG_016548.1:g.46959_46960insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355485.7:c.947-33_947-32insCTTT MANE Select	ENSP00000347672.2:n.947-33_947-32insCTTT
ENST00000310260.7:c.947-33_947-32insCTTT	ENSP00000310800.3:n.947-33_947-32insCTTT
ENST00000355485.6:c.947-33_947-32insCTTT	ENSP00000347672.2:n.947-33_947-32insCTTT
ENST00000369509.1:c.947-33_947-32insCTTT	ENSP00000358522.1:n.947-33_947-32insCTTT
ENST00000369510.8:c.941-33_941-32insCTTT	ENSP00000358523.3:n.941-33_941-32insCTTT
ENST00000474344.1:n.329-33_329-32insCTTT
ENST00000478369.5:n.231-33_231-32insCTTT
NM_001172411.1:c.941-33_941-32insCTTT	NP_001165882.1:n.941-33_941-32insCTTT
NM_001172412.1:c.947-33_947-32insCTTT	NP_001165883.1:n.947-33_947-32insCTTT
NM_138959.2:c.947-33_947-32insCTTT	NP_620409.1:n.947-33_947-32insCTTT
NM_138959.3:c.947-33_947-32insCTTT MANE Select	NP_620409.1:n.947-33_947-32insCTTT
NM_001172411.2:c.941-33_941-32insCTTT	NP_001165882.1:n.941-33_941-32insCTTT
NM_001172412.2:c.947-33_947-32insCTTT	NP_001165883.1:n.947-33_947-32insCTTT