Canonical Allele Identifier: CA351623410
Gene: WNT7A HGNC NCBI

Linked Data

gnomAD v4: 3-13854786-A-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.316T>G MANE Select ENSP00000285018.4:p.Phe106Val
ENST00000285018.4:c.316T>G ENSP00000285018.4:p.Phe106Val
NM_004625.3:c.316T>G NP_004616.2:p.Phe106Val
XM_011534090.1:c.115T>G XP_011532392.1:p.Phe39Val
XM_011534091.1:c.115T>G XP_011532393.1:p.Phe39Val
XM_011534091.2:c.115T>G XP_011532393.1:p.Phe39Val
NM_004625.4:c.316T>G MANE Select NP_004616.2:p.Phe106Val