Canonical Allele Identifier: CA1140471818

Gene: VANGL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115669142T= , CM000663.2:g.115669142T=	GRCh38
NC_000001.10:g.116211763T= , CM000663.1:g.116211763T=	GRCh37
NC_000001.9:g.116013286T=	NCBI36
NG_016548.1:g.32190T=

Transcript Alleles

HGVS	Amino-acid Change
NM_138959.3:c.812+4874T= MANE Select	NP_620409.1:n.812+4874T=
ENST00000355485.7:c.812+4874T= MANE Select	ENSP00000347672.2:n.812+4874T=
NM_001172411.1:c.806+4874T=	NP_001165882.1:n.806+4874T=
NM_001172411.2:c.806+4874T=	NP_001165882.1:n.806+4874T=
NM_001172412.1:c.812+4874T=	NP_001165883.1:n.812+4874T=
NM_001172412.2:c.812+4874T=	NP_001165883.1:n.812+4874T=
NM_138959.2:c.812+4874T=	NP_620409.1:n.812+4874T=
ENST00000310260.7:c.812+4874T=	ENSP00000310800.3:n.812+4874T=
ENST00000355485.6:c.812+4874T=	ENSP00000347672.2:n.812+4874T=
ENST00000369509.1:c.812+4874T=	ENSP00000358522.1:n.812+4874T=
ENST00000369510.8:c.806+4874T=	ENSP00000358523.3:n.806+4874T=