Canonical Allele Identifier: CA2664559429

Gene: WNT7A

Linked Data

• gnomAD v4: 3-13854702-C-CATTCTGTGCGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854702_13854703insATTCTGTGCGGTG , CM000665.2:g.13854702_13854703insATTCTGTGCGGTG	GRCh38
NC_000003.11:g.13896199_13896200insATTCTGTGCGGTG , CM000665.1:g.13896199_13896200insATTCTGTGCGGTG	GRCh37
NC_000003.10:g.13871200_13871201insATTCTGTGCGGTG	NCBI36
NG_008088.1:g.30419_30420insCACCGCACAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.399_400insCACCGCACAGAAT MANE Select	ENSP00000285018.4:p.Asp134HisfsTer5
ENST00000285018.4:c.399_400insCACCGCACAGAAT	ENSP00000285018.4:p.Asp134HisfsTer5
NM_004625.3:c.399_400insCACCGCACAGAAT	NP_004616.2:p.Asp134HisfsTer5
XM_011534090.1:c.198_199insCACCGCACAGAAT	XP_011532392.1:p.Asp67HisfsTer5
XM_011534091.1:c.198_199insCACCGCACAGAAT	XP_011532393.1:p.Asp67HisfsTer5
XM_011534091.2:c.198_199insCACCGCACAGAAT	XP_011532393.1:p.Asp67HisfsTer5
NM_004625.4:c.399_400insCACCGCACAGAAT MANE Select	NP_004616.2:p.Asp134HisfsTer5