Canonical Allele Identifier: CA351623394
Gene: WNT7A HGNC NCBI

Linked Data

gnomAD v4: 3-13854778-G-T
MyVariant Identifiers: chr3:g.13896275G>T (hg19) chr3:g.13854778G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854778G>T , CM000665.2:g.13854778G>T GRCh38
NC_000003.11:g.13896275G>T , CM000665.1:g.13896275G>T GRCh37
NC_000003.10:g.13871276G>T NCBI36
NG_008088.1:g.30344C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.324C>A MANE Select ENSP00000285018.4:p.Tyr108Ter
ENST00000285018.4:c.324C>A ENSP00000285018.4:p.Tyr108Ter
NM_004625.3:c.324C>A NP_004616.2:p.Tyr108Ter
XM_011534090.1:c.123C>A XP_011532392.1:p.Tyr41Ter
XM_011534091.1:c.123C>A XP_011532393.1:p.Tyr41Ter
XM_011534091.2:c.123C>A XP_011532393.1:p.Tyr41Ter
NM_004625.4:c.324C>A MANE Select NP_004616.2:p.Tyr108Ter
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