Canonical Allele Identifier: CA2414181946

Gene: STS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7305109C= , CM000685.2:g.7305109C=	GRCh38
NC_000023.10:g.7223150C= , CM000685.1:g.7223150C=	GRCh37
NC_000023.9:g.7233150C=	NCBI36
NG_021472.1:g.90679C=
NG_021472.2:g.162858C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001320752.2:c.1007C= MANE Select	NP_001307681.2:p.Ser336=
ENST00000674429.1:c.1007C= MANE Select	ENSP00000501534.1:p.Ser336=
NM_000351.4:c.1022C=	NP_000342.2:p.Ser341=
NM_000351.5:c.1022C=	NP_000342.2:p.Ser341=
NM_000351.7:c.1007C=	NP_000342.3:p.Ser336=
NM_001320750.1:c.1043C=	NP_001307679.1:p.Ser348=
NM_001320750.3:c.1043C=	NP_001307679.1:p.Ser348=
NM_001320751.1:c.1043C=	NP_001307680.1:p.Ser348=
NM_001320751.2:c.1043C=	NP_001307680.1:p.Ser348=
NM_001320752.1:c.1043C=	NP_001307681.1:p.Ser348=
NM_001320753.1:c.1007C=	NP_001307682.1:p.Ser336=
NM_001320753.2:c.1007C=	NP_001307682.1:p.Ser336=
NM_001320754.1:c.1007C=	NP_001307683.1:p.Ser336=
NM_001320754.2:c.1007C=	NP_001307683.1:p.Ser336=
ENST00000217961.4:c.1022C=	ENSP00000217961.4:p.Ser341=
ENST00000217961.5:c.1007C=	ENSP00000217961.5:p.Ser336=
ENST00000658154.1:n.1247C=
ENST00000660000.2:c.944-20230C=	ENSP00000499642.2:n.944-20230C=
ENST00000664306.2:c.1007C=	ENSP00000499549.2:p.Ser336=
ENST00000666110.2:c.1007C=	ENSP00000499472.2:p.Ser336=
ENST00000674499.1:c.1022C=	ENSP00000501360.1:p.Ser341=
XM_005274511.1:c.1043C=	XP_005274568.1:p.Ser348=
XM_011545515.1:c.1043C=	XP_011543817.1:p.Ser348=
XM_011545516.1:c.1043C=	XP_011543818.1:p.Ser348=
XM_011545517.1:c.1007C=	XP_011543819.1:p.Ser336=
XM_011545518.1:c.1007C=	XP_011543820.1:p.Ser336=