Canonical Allele Identifier: CA1346837704
Gene: WNT7A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854788G= , CM000665.2:g.13854788G= GRCh38
NC_000003.11:g.13896285G= , CM000665.1:g.13896285G= GRCh37
NC_000003.10:g.13871286G= NCBI36
NG_008088.1:g.30334C=

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.314C= MANE Select ENSP00000285018.4:p.Ala105=
ENST00000285018.4:c.314C= ENSP00000285018.4:p.Ala105=
NM_004625.3:c.314C= NP_004616.2:p.Ala105=
XM_011534090.1:c.113C= XP_011532392.1:p.Ala38=
XM_011534091.1:c.113C= XP_011532393.1:p.Ala38=
XM_011534091.2:c.113C= XP_011532393.1:p.Ala38=
NM_004625.4:c.314C= MANE Select NP_004616.2:p.Ala105=