Canonical Allele Identifier: CA351623212
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896190T>G (hg19) chr3:g.13854693T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854693T>G , CM000665.2:g.13854693T>G GRCh38
NC_000003.11:g.13896190T>G , CM000665.1:g.13896190T>G GRCh37
NC_000003.10:g.13871191T>G NCBI36
NG_008088.1:g.30429A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.409A>C MANE Select ENSP00000285018.4:p.Lys137Gln
ENST00000285018.4:c.409A>C ENSP00000285018.4:p.Lys137Gln
NM_004625.3:c.409A>C NP_004616.2:p.Lys137Gln
XM_011534090.1:c.208A>C XP_011532392.1:p.Lys70Gln
XM_011534091.1:c.208A>C XP_011532393.1:p.Lys70Gln
XM_011534091.2:c.208A>C XP_011532393.1:p.Lys70Gln
NM_004625.4:c.409A>C MANE Select NP_004616.2:p.Lys137Gln
Search 100 bp 5'
Search 100 bp 3'