Canonical Allele Identifier: CA351623391
Gene: WNT7A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854777C>A , CM000665.2:g.13854777C>A GRCh38
NC_000003.11:g.13896274C>A , CM000665.1:g.13896274C>A GRCh37
NC_000003.10:g.13871275C>A NCBI36
NG_008088.1:g.30345G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.325G>T MANE Select ENSP00000285018.4:p.Ala109Ser
ENST00000285018.4:c.325G>T ENSP00000285018.4:p.Ala109Ser
NM_004625.3:c.325G>T NP_004616.2:p.Ala109Ser
XM_011534090.1:c.124G>T XP_011532392.1:p.Ala42Ser
XM_011534091.1:c.124G>T XP_011532393.1:p.Ala42Ser
XM_011534091.2:c.124G>T XP_011532393.1:p.Ala42Ser
NM_004625.4:c.325G>T MANE Select NP_004616.2:p.Ala109Ser