Canonical Allele Identifier: CA351623397
Gene: WNT7A HGNC NCBI

Linked Data

dbSNP Id: rs1575068953

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854779T>G , CM000665.2:g.13854779T>G GRCh38
NC_000003.11:g.13896276T>G , CM000665.1:g.13896276T>G GRCh37
NC_000003.10:g.13871277T>G NCBI36
NG_008088.1:g.30343A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000285018.5:c.323A>C MANE Select ENSP00000285018.4:p.Tyr108Ser
ENST00000285018.4:c.323A>C ENSP00000285018.4:p.Tyr108Ser
NM_004625.3:c.323A>C NP_004616.2:p.Tyr108Ser
XM_011534090.1:c.122A>C XP_011532392.1:p.Tyr41Ser
XM_011534091.1:c.122A>C XP_011532393.1:p.Tyr41Ser
XM_011534091.2:c.122A>C XP_011532393.1:p.Tyr41Ser
NM_004625.4:c.323A>C MANE Select NP_004616.2:p.Tyr108Ser