Canonical Allele Identifier: CA2414181922

Gene: STS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7305017T= , CM000685.2:g.7305017T=	GRCh38
NC_000023.10:g.7223058T= , CM000685.1:g.7223058T=	GRCh37
NC_000023.9:g.7233058T=	NCBI36
NG_021472.1:g.90587T=
NG_021472.2:g.162766T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000217961.5:c.944-29T=	ENSP00000217961.5:n.944-29T=
ENST00000658154.1:n.1184-29T=
ENST00000660000.2:c.944-20322T=	ENSP00000499642.2:n.944-20322T=
ENST00000664306.2:c.944-29T=	ENSP00000499549.2:n.944-29T=
ENST00000666110.2:c.944-29T=	ENSP00000499472.2:n.944-29T=
ENST00000674429.1:c.944-29T= MANE Select	ENSP00000501534.1:n.944-29T=
ENST00000674499.1:c.959-29T=	ENSP00000501360.1:n.959-29T=
ENST00000217961.4:c.959-29T=	ENSP00000217961.4:n.959-29T=
NM_000351.4:c.959-29T=	NP_000342.2:n.959-29T=
XM_005274511.1:c.980-29T=	XP_005274568.1:n.980-29T=
XM_011545515.1:c.980-29T=	XP_011543817.1:n.980-29T=
XM_011545516.1:c.980-29T=	XP_011543818.1:n.980-29T=
XM_011545517.1:c.944-29T=	XP_011543819.1:n.944-29T=
XM_011545518.1:c.944-29T=	XP_011543820.1:n.944-29T=
NM_000351.5:c.959-29T=	NP_000342.2:n.959-29T=
NM_001320750.1:c.980-29T=	NP_001307679.1:n.980-29T=
NM_001320751.1:c.980-29T=	NP_001307680.1:n.980-29T=
NM_001320752.1:c.980-29T=	NP_001307681.1:n.980-29T=
NM_001320753.1:c.944-29T=	NP_001307682.1:n.944-29T=
NM_001320754.1:c.944-29T=	NP_001307683.1:n.944-29T=
NM_000351.7:c.944-29T=	NP_000342.3:n.944-29T=
NM_001320750.3:c.980-29T=	NP_001307679.1:n.980-29T=
NM_001320751.2:c.980-29T=	NP_001307680.1:n.980-29T=
NM_001320752.2:c.944-29T= MANE Select	NP_001307681.2:n.944-29T=
NM_001320753.2:c.944-29T=	NP_001307682.1:n.944-29T=
NM_001320754.2:c.944-29T=	NP_001307683.1:n.944-29T=