Canonical Allele Identifier: CA351623379

Gene: WNT7A

Linked Data

• MyVariant Identifiers: chr3:g.13896268T>A (hg19) ; chr3:g.13854771T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13854771T>A , CM000665.2:g.13854771T>A	GRCh38
NC_000003.11:g.13896268T>A , CM000665.1:g.13896268T>A	GRCh37
NC_000003.10:g.13871269T>A	NCBI36
NG_008088.1:g.30351A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285018.5:c.331A>T MANE Select	ENSP00000285018.4:p.Ile111Phe
ENST00000285018.4:c.331A>T	ENSP00000285018.4:p.Ile111Phe
NM_004625.3:c.331A>T	NP_004616.2:p.Ile111Phe
XM_011534090.1:c.130A>T	XP_011532392.1:p.Ile44Phe
XM_011534091.1:c.130A>T	XP_011532393.1:p.Ile44Phe
XM_011534091.2:c.130A>T	XP_011532393.1:p.Ile44Phe
NM_004625.4:c.331A>T MANE Select	NP_004616.2:p.Ile111Phe