Canonical Allele Identifier: CA1346837666

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854777C= , CM000665.2:g.13854777C=	GRCh38
NC_000003.11:g.13896274C= , CM000665.1:g.13896274C=	GRCh37
NC_000003.10:g.13871275C=	NCBI36
NG_008088.1:g.30345G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.325G= MANE Select	ENSP00000285018.4:p.Ala109=
ENST00000285018.4:c.325G=	ENSP00000285018.4:p.Ala109=
NM_004625.3:c.325G=	NP_004616.2:p.Ala109=
XM_011534090.1:c.124G=	XP_011532392.1:p.Ala42=
XM_011534091.1:c.124G=	XP_011532393.1:p.Ala42=
XM_011534091.2:c.124G=	XP_011532393.1:p.Ala42=
NM_004625.4:c.325G= MANE Select	NP_004616.2:p.Ala109=