Canonical Allele Identifier: CA660577410
Gene: NANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1472619065
gnomAD v4: 10-119030041-CTCG-C
MyVariant Identifiers: chr10:g.120789554_120789556del (hg19) chr10:g.119030042_119030044del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119030047_119030049del , CM000672.2:g.119030047_119030049del GRCh38
NC_000010.10:g.120789559_120789561del , CM000672.1:g.120789559_120789561del GRCh37
NC_000010.9:g.120779549_120779551del NCBI36
NG_050764.1:g.5332_5334del

Transcript Alleles

HGVS Amino-acid Change
ENST00000425699.3:c.246_248del MANE Select ENSP00000393275.1:p.Ser83del
ENST00000425699.2:c.246_248del ENSP00000393275.1:p.Ser83del
NM_199461.2:c.246_248del NP_955631.1:p.Ser83del
NM_199461.3:c.246_248del NP_955631.1:p.Ser83del
NM_199461.4:c.246_248del MANE Select NP_955631.1:p.Ser83del
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