Canonical Allele Identifier: CA121124
Gene: STS HGNC NCBI

Linked Data

ClinVar Variation Id: 10556
ClinVar RCV Id: RCV000011302
dbSNP Id: rs137853169

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.7334060A>G , CM000685.2:g.7334060A>G GRCh38
NC_000023.10:g.7252101A>G , CM000685.1:g.7252101A>G GRCh37
NC_000023.9:g.7262101A>G NCBI36
NG_021472.1:g.119630A>G
NG_021472.2:g.191809A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000217961.5:c.1316A>G ENSP00000217961.5:p.His439Arg
ENST00000658154.1:n.1556A>G
ENST00000660000.2:c.1178A>G ENSP00000499642.2:p.His393Arg
ENST00000664306.2:c.1316A>G ENSP00000499549.2:p.His439Arg
ENST00000666110.2:c.1316A>G ENSP00000499472.2:p.His439Arg
ENST00000674429.1:c.1316A>G MANE Select ENSP00000501534.1:p.His439Arg
ENST00000674499.1:c.1331A>G ENSP00000501360.1:p.His444Arg
ENST00000217961.4:c.1331A>G ENSP00000217961.4:p.His444Arg
NM_000351.4:c.1331A>G NP_000342.2:p.His444Arg
XM_005274511.1:c.1352A>G XP_005274568.1:p.His451Arg
XM_011545515.1:c.1352A>G XP_011543817.1:p.His451Arg
XM_011545516.1:c.1352A>G XP_011543818.1:p.His451Arg
XM_011545517.1:c.1316A>G XP_011543819.1:p.His439Arg
XM_011545518.1:c.1316A>G XP_011543820.1:p.His439Arg
NM_000351.5:c.1331A>G NP_000342.2:p.His444Arg
NM_001320750.1:c.1352A>G NP_001307679.1:p.His451Arg
NM_001320751.1:c.1352A>G NP_001307680.1:p.His451Arg
NM_001320752.1:c.1352A>G NP_001307681.1:p.His451Arg
NM_001320753.1:c.1316A>G NP_001307682.1:p.His439Arg
NM_001320754.1:c.1316A>G NP_001307683.1:p.His439Arg
NM_000351.7:c.1316A>G NP_000342.3:p.His439Arg
NM_001320750.3:c.1352A>G NP_001307679.1:p.His451Arg
NM_001320751.2:c.1352A>G NP_001307680.1:p.His451Arg
NM_001320752.2:c.1316A>G MANE Select NP_001307681.2:p.His439Arg
NM_001320753.2:c.1316A>G NP_001307682.1:p.His439Arg
NM_001320754.2:c.1316A>G NP_001307683.1:p.His439Arg