Canonical Allele Identifier: CA351623413
Gene: WNT7A HGNC NCBI

Linked Data

gnomAD v4: 3-13854788-G-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.314C>G MANE Select ENSP00000285018.4:p.Ala105Gly
ENST00000285018.4:c.314C>G ENSP00000285018.4:p.Ala105Gly
NM_004625.3:c.314C>G NP_004616.2:p.Ala105Gly
XM_011534090.1:c.113C>G XP_011532392.1:p.Ala38Gly
XM_011534091.1:c.113C>G XP_011532393.1:p.Ala38Gly
XM_011534091.2:c.113C>G XP_011532393.1:p.Ala38Gly
NM_004625.4:c.314C>G MANE Select NP_004616.2:p.Ala105Gly