Canonical Allele Identifier: CA432695614
Gene: WNT7A HGNC NCBI

Linked Data

gnomAD v4: 3-13854769-A-G
MyVariant Identifiers: chr3:g.13896266A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854769A>G , CM000665.2:g.13854769A>G GRCh38
NC_000003.11:g.13896266A>G , CM000665.1:g.13896266A>G GRCh37
NC_000003.10:g.13871267A>G NCBI36
NG_008088.1:g.30353T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.333T>C MANE Select ENSP00000285018.4:p.Ile111=
ENST00000285018.4:c.333T>C ENSP00000285018.4:p.Ile111=
NM_004625.3:c.333T>C NP_004616.2:p.Ile111=
XM_011534090.1:c.132T>C XP_011532392.1:p.Ile44=
XM_011534091.1:c.132T>C XP_011532393.1:p.Ile44=
XM_011534091.2:c.132T>C XP_011532393.1:p.Ile44=
NM_004625.4:c.333T>C MANE Select NP_004616.2:p.Ile111=