Canonical Allele Identifier: CA1346837694

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854784G= , CM000665.2:g.13854784G=	GRCh38
NC_000003.11:g.13896281G= , CM000665.1:g.13896281G=	GRCh37
NC_000003.10:g.13871282G=	NCBI36
NG_008088.1:g.30338C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.318C= MANE Select	ENSP00000285018.4:p.Phe106=
ENST00000285018.4:c.318C=	ENSP00000285018.4:p.Phe106=
NM_004625.3:c.318C=	NP_004616.2:p.Phe106=
XM_011534090.1:c.117C=	XP_011532392.1:p.Phe39=
XM_011534091.1:c.117C=	XP_011532393.1:p.Phe39=
XM_011534091.2:c.117C=	XP_011532393.1:p.Phe39=
NM_004625.4:c.318C= MANE Select	NP_004616.2:p.Phe106=