Canonical Allele Identifier: CA1346837673

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854778G= , CM000665.2:g.13854778G=	GRCh38
NC_000003.11:g.13896275G= , CM000665.1:g.13896275G=	GRCh37
NC_000003.10:g.13871276G=	NCBI36
NG_008088.1:g.30344C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.324C= MANE Select	ENSP00000285018.4:p.Tyr108=
ENST00000285018.4:c.324C=	ENSP00000285018.4:p.Tyr108=
NM_004625.3:c.324C=	NP_004616.2:p.Tyr108=
XM_011534090.1:c.123C=	XP_011532392.1:p.Tyr41=
XM_011534091.1:c.123C=	XP_011532393.1:p.Tyr41=
XM_011534091.2:c.123C=	XP_011532393.1:p.Tyr41=
NM_004625.4:c.324C= MANE Select	NP_004616.2:p.Tyr108=