Canonical Allele Identifier: CA1190697372

Gene: VANGL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115664075C= , CM000663.2:g.115664075C=	GRCh38
NC_000001.10:g.116206696C= , CM000663.1:g.116206696C=	GRCh37
NC_000001.9:g.116008219C=	NCBI36
NG_016548.1:g.27123C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355485.7:c.619C= MANE Select	ENSP00000347672.2:p.Arg207=
ENST00000310260.7:c.619C=	ENSP00000310800.3:p.Arg207=
ENST00000355485.6:c.619C=	ENSP00000347672.2:p.Arg207=
ENST00000369509.1:c.619C=	ENSP00000358522.1:p.Arg207=
ENST00000369510.8:c.613C=	ENSP00000358523.3:p.Arg205=
NM_001172411.1:c.613C=	NP_001165882.1:p.Arg205=
NM_001172412.1:c.619C=	NP_001165883.1:p.Arg207=
NM_138959.2:c.619C=	NP_620409.1:p.Arg207=
NM_138959.3:c.619C= MANE Select	NP_620409.1:p.Arg207=
NM_001172411.2:c.613C=	NP_001165882.1:p.Arg205=
NM_001172412.2:c.619C=	NP_001165883.1:p.Arg207=