Canonical Allele Identifier: CA341763143

Gene: VANGL1

Linked Data

• MyVariant Identifiers: chr1:g.116206702T>A (hg19) ; chr1:g.115664081T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115664081T>A , CM000663.2:g.115664081T>A	GRCh38
NC_000001.10:g.116206702T>A , CM000663.1:g.116206702T>A	GRCh37
NC_000001.9:g.116008225T>A	NCBI36
NG_016548.1:g.27129T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355485.7:c.625T>A MANE Select	ENSP00000347672.2:p.Leu209Met
ENST00000310260.7:c.625T>A	ENSP00000310800.3:p.Leu209Met
ENST00000355485.6:c.625T>A	ENSP00000347672.2:p.Leu209Met
ENST00000369509.1:c.625T>A	ENSP00000358522.1:p.Leu209Met
ENST00000369510.8:c.619T>A	ENSP00000358523.3:p.Leu207Met
NM_001172411.1:c.619T>A	NP_001165882.1:p.Leu207Met
NM_001172412.1:c.625T>A	NP_001165883.1:p.Leu209Met
NM_138959.2:c.625T>A	NP_620409.1:p.Leu209Met
NM_138959.3:c.625T>A MANE Select	NP_620409.1:p.Leu209Met
NM_001172411.2:c.619T>A	NP_001165882.1:p.Leu207Met
NM_001172412.2:c.625T>A	NP_001165883.1:p.Leu209Met