Canonical Allele Identifier: CA2266565

Gene: WNT7A

Linked Data

• ClinVar Variation Id: 281770
• ClinVar RCV Id: RCV000273739 ; RCV000883704 ; RCV003977734
• dbSNP Id: rs35103037
• ExAC: 3:13916667 G / A
• gnomAD v2: 3-13916667-G-A
• gnomAD v3: 3-13875170-G-A
• gnomAD v4: 3-13875170-G-A
• MyVariant Identifiers: chr3:g.13916667G>A (hg19) ; chr3:g.13875170G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13875170G>A , CM000665.2:g.13875170G>A	GRCh38
NC_000003.11:g.13916667G>A , CM000665.1:g.13916667G>A	GRCh37
NC_000003.10:g.13891668G>A	NCBI36
NG_008088.1:g.9952C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.75C>T MANE Select	ENSP00000285018.4:p.Gly25=
ENST00000285018.4:c.75C>T	ENSP00000285018.4:p.Gly25=
ENST00000497808.1:n.307C>T
NM_004625.3:c.75C>T	NP_004616.2:p.Gly25=
XM_011534090.1:c.-127C>T	XP_011532392.1:n.-127C>T
XM_011534091.1:c.-127C>T	XP_011532393.1:n.-127C>T
XM_011534091.2:c.-127C>T	XP_011532393.1:n.-127C>T
NM_004625.4:c.75C>T MANE Select	NP_004616.2:p.Gly25=