Canonical Allele Identifier: CA1346837680

Gene: WNT7A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854781G= , CM000665.2:g.13854781G=	GRCh38
NC_000003.11:g.13896278G= , CM000665.1:g.13896278G=	GRCh37
NC_000003.10:g.13871279G=	NCBI36
NG_008088.1:g.30341C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000285018.5:c.321C= MANE Select	ENSP00000285018.4:p.Thr107=
ENST00000285018.4:c.321C=	ENSP00000285018.4:p.Thr107=
NM_004625.3:c.321C=	NP_004616.2:p.Thr107=
XM_011534090.1:c.120C=	XP_011532392.1:p.Thr40=
XM_011534091.1:c.120C=	XP_011532393.1:p.Thr40=
XM_011534091.2:c.120C=	XP_011532393.1:p.Thr40=
NM_004625.4:c.321C= MANE Select	NP_004616.2:p.Thr107=