Canonical Allele Identifier: CA351623412
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896283A>T (hg19) chr3:g.13854786A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854786A>T , CM000665.2:g.13854786A>T GRCh38
NC_000003.11:g.13896283A>T , CM000665.1:g.13896283A>T GRCh37
NC_000003.10:g.13871284A>T NCBI36
NG_008088.1:g.30336T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.316T>A MANE Select ENSP00000285018.4:p.Phe106Ile
ENST00000285018.4:c.316T>A ENSP00000285018.4:p.Phe106Ile
NM_004625.3:c.316T>A NP_004616.2:p.Phe106Ile
XM_011534090.1:c.115T>A XP_011532392.1:p.Phe39Ile
XM_011534091.1:c.115T>A XP_011532393.1:p.Phe39Ile
XM_011534091.2:c.115T>A XP_011532393.1:p.Phe39Ile
NM_004625.4:c.316T>A MANE Select NP_004616.2:p.Phe106Ile
Search 100 bp 5'
Search 100 bp 3'