Canonical Allele Identifier: CA419892589

Gene: VANGL1

Linked Data

• MyVariant Identifiers: chr1:g.116226587C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115683966C>G , CM000663.2:g.115683966C>G	GRCh38
NC_000001.10:g.116226587C>G , CM000663.1:g.116226587C>G	GRCh37
NC_000001.9:g.116028110C>G	NCBI36
NG_016548.1:g.47014C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355485.7:c.969C>G MANE Select	ENSP00000347672.2:p.Gly323=
ENST00000310260.7:c.969C>G	ENSP00000310800.3:p.Gly323=
ENST00000355485.6:c.969C>G	ENSP00000347672.2:p.Gly323=
ENST00000369509.1:c.969C>G	ENSP00000358522.1:p.Gly323=
ENST00000369510.8:c.963C>G	ENSP00000358523.3:p.Gly321=
ENST00000474344.1:n.351C>G
ENST00000478369.5:n.253C>G
NM_001172411.1:c.963C>G	NP_001165882.1:p.Gly321=
NM_001172412.1:c.969C>G	NP_001165883.1:p.Gly323=
NM_138959.2:c.969C>G	NP_620409.1:p.Gly323=
NM_138959.3:c.969C>G MANE Select	NP_620409.1:p.Gly323=
NM_001172411.2:c.963C>G	NP_001165882.1:p.Gly321=
NM_001172412.2:c.969C>G	NP_001165883.1:p.Gly323=