Canonical Allele Identifier: CA351623366

Gene: WNT7A

Linked Data

• MyVariant Identifiers: chr3:g.13896261G>T (hg19) ; chr3:g.13854764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854764G>T , CM000665.2:g.13854764G>T	GRCh38
NC_000003.11:g.13896261G>T , CM000665.1:g.13896261G>T	GRCh37
NC_000003.10:g.13871262G>T	NCBI36
NG_008088.1:g.30358C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.338C>A MANE Select	ENSP00000285018.4:p.Ala113Asp
ENST00000285018.4:c.338C>A	ENSP00000285018.4:p.Ala113Asp
NM_004625.3:c.338C>A	NP_004616.2:p.Ala113Asp
XM_011534090.1:c.137C>A	XP_011532392.1:p.Ala46Asp
XM_011534091.1:c.137C>A	XP_011532393.1:p.Ala46Asp
XM_011534091.2:c.137C>A	XP_011532393.1:p.Ala46Asp
NM_004625.4:c.338C>A MANE Select	NP_004616.2:p.Ala113Asp