Canonical Allele Identifier: CA351623316
Gene: WNT7A HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.13896235C>G (hg19) chr3:g.13854738C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854738C>G , CM000665.2:g.13854738C>G GRCh38
NC_000003.11:g.13896235C>G , CM000665.1:g.13896235C>G GRCh37
NC_000003.10:g.13871236C>G NCBI36
NG_008088.1:g.30384G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.364G>C MANE Select ENSP00000285018.4:p.Ala122Pro
ENST00000285018.4:c.364G>C ENSP00000285018.4:p.Ala122Pro
NM_004625.3:c.364G>C NP_004616.2:p.Ala122Pro
XM_011534090.1:c.163G>C XP_011532392.1:p.Ala55Pro
XM_011534091.1:c.163G>C XP_011532393.1:p.Ala55Pro
XM_011534091.2:c.163G>C XP_011532393.1:p.Ala55Pro
NM_004625.4:c.364G>C MANE Select NP_004616.2:p.Ala122Pro
Search 100 bp 5'
Search 100 bp 3'