Canonical Allele Identifier: CA1346837467
Gene: WNT7A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.13854682_13854689delinsCTGGCCTT , CM000665.2:g.13854682_13854689delinsCTGGCCTT GRCh38
NC_000003.11:g.13896179_13896186delinsCTGGCCTT , CM000665.1:g.13896179_13896186delinsCTGGCCTT GRCh37
NC_000003.10:g.13871180_13871187delinsCTGGCCTT NCBI36
NG_008088.1:g.30433_30440delinsAAGGCCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000285018.5:c.413_420delinsAAGGCCAG MANE Select ENSP00000285018.4:p.Gln138=
ENST00000285018.4:c.413_420delinsAAGGCCAG ENSP00000285018.4:p.Gln138=
NM_004625.3:c.413_420delinsAAGGCCAG NP_004616.2:p.Gln138=
XM_011534090.1:c.212_219delinsAAGGCCAG XP_011532392.1:p.Gln71=
XM_011534091.1:c.212_219delinsAAGGCCAG XP_011532393.1:p.Gln71=
XM_011534091.2:c.212_219delinsAAGGCCAG XP_011532393.1:p.Gln71=
NM_004625.4:c.413_420delinsAAGGCCAG MANE Select NP_004616.2:p.Gln138=
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