Canonical Allele Identifier: CA351623396
Gene: WNT7A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854779T>C , CM000665.2:g.13854779T>C GRCh38
NC_000003.11:g.13896276T>C , CM000665.1:g.13896276T>C GRCh37
NC_000003.10:g.13871277T>C NCBI36
NG_008088.1:g.30343A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.323A>G MANE Select ENSP00000285018.4:p.Tyr108Cys
ENST00000285018.4:c.323A>G ENSP00000285018.4:p.Tyr108Cys
NM_004625.3:c.323A>G NP_004616.2:p.Tyr108Cys
XM_011534090.1:c.122A>G XP_011532392.1:p.Tyr41Cys
XM_011534091.1:c.122A>G XP_011532393.1:p.Tyr41Cys
XM_011534091.2:c.122A>G XP_011532393.1:p.Tyr41Cys
NM_004625.4:c.323A>G MANE Select NP_004616.2:p.Tyr108Cys