Canonical Allele Identifier: CA412022353

Gene: STS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7325356T>C , CM000685.2:g.7325356T>C	GRCh38
NC_000023.10:g.7243397T>C , CM000685.1:g.7243397T>C	GRCh37
NC_000023.9:g.7253397T>C	NCBI36
NG_021472.1:g.110926T>C
NG_021472.2:g.183105T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001320752.2:c.1099T>C MANE Select	NP_001307681.2:p.Trp367Arg
ENST00000674429.1:c.1099T>C MANE Select	ENSP00000501534.1:p.Trp367Arg
NM_000351.4:c.1114T>C	NP_000342.2:p.Trp372Arg
NM_000351.5:c.1114T>C	NP_000342.2:p.Trp372Arg
NM_000351.7:c.1099T>C	NP_000342.3:p.Trp367Arg
NM_001320750.1:c.1135T>C	NP_001307679.1:p.Trp379Arg
NM_001320750.3:c.1135T>C	NP_001307679.1:p.Trp379Arg
NM_001320751.1:c.1135T>C	NP_001307680.1:p.Trp379Arg
NM_001320751.2:c.1135T>C	NP_001307680.1:p.Trp379Arg
NM_001320752.1:c.1135T>C	NP_001307681.1:p.Trp379Arg
NM_001320753.1:c.1099T>C	NP_001307682.1:p.Trp367Arg
NM_001320753.2:c.1099T>C	NP_001307682.1:p.Trp367Arg
NM_001320754.1:c.1099T>C	NP_001307683.1:p.Trp367Arg
NM_001320754.2:c.1099T>C	NP_001307683.1:p.Trp367Arg
ENST00000217961.4:c.1114T>C	ENSP00000217961.4:p.Trp372Arg
ENST00000217961.5:c.1099T>C	ENSP00000217961.5:p.Trp367Arg
ENST00000658154.1:n.1339T>C
ENST00000660000.2:c.961T>C	ENSP00000499642.2:p.Trp321Arg
ENST00000664306.2:c.1099T>C	ENSP00000499549.2:p.Trp367Arg
ENST00000666110.2:c.1099T>C	ENSP00000499472.2:p.Trp367Arg
ENST00000674499.1:c.1114T>C	ENSP00000501360.1:p.Trp372Arg
XM_005274511.1:c.1135T>C	XP_005274568.1:p.Trp379Arg
XM_011545515.1:c.1135T>C	XP_011543817.1:p.Trp379Arg
XM_011545516.1:c.1135T>C	XP_011543818.1:p.Trp379Arg
XM_011545517.1:c.1099T>C	XP_011543819.1:p.Trp367Arg
XM_011545518.1:c.1099T>C	XP_011543820.1:p.Trp367Arg