Canonical Allele Identifier: CA351623409
Gene: WNT7A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854785A>T , CM000665.2:g.13854785A>T GRCh38
NC_000003.11:g.13896282A>T , CM000665.1:g.13896282A>T GRCh37
NC_000003.10:g.13871283A>T NCBI36
NG_008088.1:g.30337T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.317T>A MANE Select ENSP00000285018.4:p.Phe106Tyr
ENST00000285018.4:c.317T>A ENSP00000285018.4:p.Phe106Tyr
NM_004625.3:c.317T>A NP_004616.2:p.Phe106Tyr
XM_011534090.1:c.116T>A XP_011532392.1:p.Phe39Tyr
XM_011534091.1:c.116T>A XP_011532393.1:p.Phe39Tyr
XM_011534091.2:c.116T>A XP_011532393.1:p.Phe39Tyr
NM_004625.4:c.317T>A MANE Select NP_004616.2:p.Phe106Tyr