Canonical Allele Identifier: CA2414189592

Gene: STS

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_001320752.2:c.1099T= MANE Select	NP_001307681.2:p.Trp367=
ENST00000674429.1:c.1099T= MANE Select	ENSP00000501534.1:p.Trp367=
NM_000351.4:c.1114T=	NP_000342.2:p.Trp372=
NM_000351.5:c.1114T=	NP_000342.2:p.Trp372=
NM_000351.7:c.1099T=	NP_000342.3:p.Trp367=
NM_001320750.1:c.1135T=	NP_001307679.1:p.Trp379=
NM_001320750.3:c.1135T=	NP_001307679.1:p.Trp379=
NM_001320751.1:c.1135T=	NP_001307680.1:p.Trp379=
NM_001320751.2:c.1135T=	NP_001307680.1:p.Trp379=
NM_001320752.1:c.1135T=	NP_001307681.1:p.Trp379=
NM_001320753.1:c.1099T=	NP_001307682.1:p.Trp367=
NM_001320753.2:c.1099T=	NP_001307682.1:p.Trp367=
NM_001320754.1:c.1099T=	NP_001307683.1:p.Trp367=
NM_001320754.2:c.1099T=	NP_001307683.1:p.Trp367=
ENST00000217961.4:c.1114T=	ENSP00000217961.4:p.Trp372=
ENST00000217961.5:c.1099T=	ENSP00000217961.5:p.Trp367=
ENST00000658154.1:n.1339T=
ENST00000660000.2:c.961T=	ENSP00000499642.2:p.Trp321=
ENST00000664306.2:c.1099T=	ENSP00000499549.2:p.Trp367=
ENST00000666110.2:c.1099T=	ENSP00000499472.2:p.Trp367=
ENST00000674499.1:c.1114T=	ENSP00000501360.1:p.Trp372=
XM_005274511.1:c.1135T=	XP_005274568.1:p.Trp379=
XM_011545515.1:c.1135T=	XP_011543817.1:p.Trp379=
XM_011545516.1:c.1135T=	XP_011543818.1:p.Trp379=
XM_011545517.1:c.1099T=	XP_011543819.1:p.Trp367=
XM_011545518.1:c.1099T=	XP_011543820.1:p.Trp367=