Canonical Allele Identifier: CA326423563
Gene: STS HGNC NCBI

Linked Data

dbSNP Id: rs5933863
gnomAD v2: X-7270694-G-A
gnomAD v3: X-7352653-G-A
gnomAD v4: X-7352653-G-A
MyVariant Identifiers: chrX:g.7270694G>A (hg19) chrX:g.7352653G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.7352653G>A , CM000685.2:g.7352653G>A GRCh38
NC_000023.10:g.7270694G>A , CM000685.1:g.7270694G>A GRCh37
NC_000023.9:g.7280694G>A NCBI36
NG_021472.1:g.138223G>A
NG_021472.2:g.210402G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217961.5:c.*2392G>A ENSP00000217961.5:n.*2392G>A
ENST00000658154.1:n.1603+18546G>A
ENST00000660000.2:c.1225+18546G>A ENSP00000499642.2:n.1225+18546G>A
ENST00000664306.2:c.1363+18546G>A ENSP00000499549.2:n.1363+18546G>A
ENST00000666110.2:c.*2392G>A ENSP00000499472.2:n.*2392G>A
ENST00000674429.1:c.*2392G>A MANE Select ENSP00000501534.1:n.*2392G>A
ENST00000674499.1:c.*2392G>A ENSP00000501360.1:n.*2392G>A
ENST00000217961.4:c.*2392G>A ENSP00000217961.4:n.*2392G>A
NM_000351.4:c.*2392G>A NP_000342.2:n.*2392G>A
XM_005274511.1:c.*2392G>A XP_005274568.1:n.*2392G>A
XM_011545515.1:c.*2392G>A XP_011543817.1:n.*2392G>A
XM_011545516.1:c.*2392G>A XP_011543818.1:n.*2392G>A
XM_011545517.1:c.*2392G>A XP_011543819.1:n.*2392G>A
XM_011545518.1:c.*2392G>A XP_011543820.1:n.*2392G>A
NM_000351.5:c.*2392G>A NP_000342.2:n.*2392G>A
NM_001320750.1:c.*2392G>A NP_001307679.1:n.*2392G>A
NM_001320751.1:c.*2392G>A NP_001307680.1:n.*2392G>A
NM_001320752.1:c.*2392G>A NP_001307681.1:n.*2392G>A
NM_001320753.1:c.*2392G>A NP_001307682.1:n.*2392G>A
NM_001320754.1:c.*2392G>A NP_001307683.1:n.*2392G>A
NM_000351.7:c.*2392G>A NP_000342.3:n.*2392G>A
NM_001320750.3:c.*2392G>A NP_001307679.1:n.*2392G>A
NM_001320751.2:c.*2392G>A NP_001307680.1:n.*2392G>A
NM_001320752.2:c.*2392G>A MANE Select NP_001307681.2:n.*2392G>A
NM_001320753.2:c.*2392G>A NP_001307682.1:n.*2392G>A
NM_001320754.2:c.*2392G>A NP_001307683.1:n.*2392G>A
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