Canonical Allele Identifier: CA351623242

Gene: WNT7A

Linked Data

• MyVariant Identifiers: chr3:g.13896202A>T (hg19) ; chr3:g.13854705A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854705A>T , CM000665.2:g.13854705A>T	GRCh38
NC_000003.11:g.13896202A>T , CM000665.1:g.13896202A>T	GRCh37
NC_000003.10:g.13871203A>T	NCBI36
NG_008088.1:g.30417T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.397T>A MANE Select	ENSP00000285018.4:p.Cys133Ser
ENST00000285018.4:c.397T>A	ENSP00000285018.4:p.Cys133Ser
NM_004625.3:c.397T>A	NP_004616.2:p.Cys133Ser
XM_011534090.1:c.196T>A	XP_011532392.1:p.Cys66Ser
XM_011534091.1:c.196T>A	XP_011532393.1:p.Cys66Ser
XM_011534091.2:c.196T>A	XP_011532393.1:p.Cys66Ser
NM_004625.4:c.397T>A MANE Select	NP_004616.2:p.Cys133Ser