Canonical Allele Identifier: CA1346837676

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854779T= , CM000665.2:g.13854779T=	GRCh38
NC_000003.11:g.13896276T= , CM000665.1:g.13896276T=	GRCh37
NC_000003.10:g.13871277T=	NCBI36
NG_008088.1:g.30343A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.323A= MANE Select	ENSP00000285018.4:p.Tyr108=
ENST00000285018.4:c.323A=	ENSP00000285018.4:p.Tyr108=
NM_004625.3:c.323A=	NP_004616.2:p.Tyr108=
XM_011534090.1:c.122A=	XP_011532392.1:p.Tyr41=
XM_011534091.1:c.122A=	XP_011532393.1:p.Tyr41=
XM_011534091.2:c.122A=	XP_011532393.1:p.Tyr41=
NM_004625.4:c.323A= MANE Select	NP_004616.2:p.Tyr108=