Canonical Allele Identifier: CA1190705868

Gene: VANGL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115683987T= , CM000663.2:g.115683987T=	GRCh38
NC_000001.10:g.116226608T= , CM000663.1:g.116226608T=	GRCh37
NC_000001.9:g.116028131T=	NCBI36
NG_016548.1:g.47035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355485.7:c.990T= MANE Select	ENSP00000347672.2:p.Ala330=
ENST00000310260.7:c.990T=	ENSP00000310800.3:p.Ala330=
ENST00000355485.6:c.990T=	ENSP00000347672.2:p.Ala330=
ENST00000369509.1:c.990T=	ENSP00000358522.1:p.Ala330=
ENST00000369510.8:c.984T=	ENSP00000358523.3:p.Ala328=
ENST00000474344.1:n.372T=
ENST00000478369.5:n.274T=
NM_001172411.1:c.984T=	NP_001165882.1:p.Ala328=
NM_001172412.1:c.990T=	NP_001165883.1:p.Ala330=
NM_138959.2:c.990T=	NP_620409.1:p.Ala330=
NM_138959.3:c.990T= MANE Select	NP_620409.1:p.Ala330=
NM_001172411.2:c.984T=	NP_001165882.1:p.Ala328=
NM_001172412.2:c.990T=	NP_001165883.1:p.Ala330=