Canonical Allele Identifier: CA351623402
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896280T>C (hg19) chr3:g.13854783T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854783T>C , CM000665.2:g.13854783T>C GRCh38
NC_000003.11:g.13896280T>C , CM000665.1:g.13896280T>C GRCh37
NC_000003.10:g.13871281T>C NCBI36
NG_008088.1:g.30339A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.319A>G MANE Select ENSP00000285018.4:p.Thr107Ala
ENST00000285018.4:c.319A>G ENSP00000285018.4:p.Thr107Ala
NM_004625.3:c.319A>G NP_004616.2:p.Thr107Ala
XM_011534090.1:c.118A>G XP_011532392.1:p.Thr40Ala
XM_011534091.1:c.118A>G XP_011532393.1:p.Thr40Ala
XM_011534091.2:c.118A>G XP_011532393.1:p.Thr40Ala
NM_004625.4:c.319A>G MANE Select NP_004616.2:p.Thr107Ala
Search 100 bp 5'
Search 100 bp 3'