Canonical Allele Identifier: CA351623275
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896217G>C (hg19) chr3:g.13854720G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854720G>C , CM000665.2:g.13854720G>C GRCh38
NC_000003.11:g.13896217G>C , CM000665.1:g.13896217G>C GRCh37
NC_000003.10:g.13871218G>C NCBI36
NG_008088.1:g.30402C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.382C>G MANE Select ENSP00000285018.4:p.Leu128Val
ENST00000285018.4:c.382C>G ENSP00000285018.4:p.Leu128Val
NM_004625.3:c.382C>G NP_004616.2:p.Leu128Val
XM_011534090.1:c.181C>G XP_011532392.1:p.Leu61Val
XM_011534091.1:c.181C>G XP_011532393.1:p.Leu61Val
XM_011534091.2:c.181C>G XP_011532393.1:p.Leu61Val
NM_004625.4:c.382C>G MANE Select NP_004616.2:p.Leu128Val
Search 100 bp 5'
Search 100 bp 3'