Canonical Allele Identifier: CA432695623
Gene: WNT7A HGNC NCBI

Linked Data

gnomAD v4: 3-13854787-C-A
MyVariant Identifiers: chr3:g.13896284C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854787C>A , CM000665.2:g.13854787C>A GRCh38
NC_000003.11:g.13896284C>A , CM000665.1:g.13896284C>A GRCh37
NC_000003.10:g.13871285C>A NCBI36
NG_008088.1:g.30335G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.315G>T MANE Select ENSP00000285018.4:p.Ala105=
ENST00000285018.4:c.315G>T ENSP00000285018.4:p.Ala105=
NM_004625.3:c.315G>T NP_004616.2:p.Ala105=
XM_011534090.1:c.114G>T XP_011532392.1:p.Ala38=
XM_011534091.1:c.114G>T XP_011532393.1:p.Ala38=
XM_011534091.2:c.114G>T XP_011532393.1:p.Ala38=
NM_004625.4:c.315G>T MANE Select NP_004616.2:p.Ala105=
Search 100 bp 5'
Search 100 bp 3'