Canonical Allele Identifier: CA412021663

Gene: STS

Linked Data

• MyVariant Identifiers: chrX:g.7223085A>T (hg19) ; chrX:g.7305044A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7305044A>T , CM000685.2:g.7305044A>T	GRCh38
NC_000023.10:g.7223085A>T , CM000685.1:g.7223085A>T	GRCh37
NC_000023.9:g.7233085A>T	NCBI36
NG_021472.1:g.90614A>T
NG_021472.2:g.162793A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000217961.5:c.944-2A>T	ENSP00000217961.5:n.944-2A>T
ENST00000658154.1:n.1184-2A>T
ENST00000660000.2:c.944-20295A>T	ENSP00000499642.2:n.944-20295A>T
ENST00000664306.2:c.944-2A>T	ENSP00000499549.2:n.944-2A>T
ENST00000666110.2:c.944-2A>T	ENSP00000499472.2:n.944-2A>T
ENST00000674429.1:c.944-2A>T MANE Select	ENSP00000501534.1:n.944-2A>T
ENST00000674499.1:c.959-2A>T	ENSP00000501360.1:n.959-2A>T
ENST00000217961.4:c.959-2A>T	ENSP00000217961.4:n.959-2A>T
NM_000351.4:c.959-2A>T	NP_000342.2:n.959-2A>T
XM_005274511.1:c.980-2A>T	XP_005274568.1:n.980-2A>T
XM_011545515.1:c.980-2A>T	XP_011543817.1:n.980-2A>T
XM_011545516.1:c.980-2A>T	XP_011543818.1:n.980-2A>T
XM_011545517.1:c.944-2A>T	XP_011543819.1:n.944-2A>T
XM_011545518.1:c.944-2A>T	XP_011543820.1:n.944-2A>T
NM_000351.5:c.959-2A>T	NP_000342.2:n.959-2A>T
NM_001320750.1:c.980-2A>T	NP_001307679.1:n.980-2A>T
NM_001320751.1:c.980-2A>T	NP_001307680.1:n.980-2A>T
NM_001320752.1:c.980-2A>T	NP_001307681.1:n.980-2A>T
NM_001320753.1:c.944-2A>T	NP_001307682.1:n.944-2A>T
NM_001320754.1:c.944-2A>T	NP_001307683.1:n.944-2A>T
NM_000351.7:c.944-2A>T	NP_000342.3:n.944-2A>T
NM_001320750.3:c.980-2A>T	NP_001307679.1:n.980-2A>T
NM_001320751.2:c.980-2A>T	NP_001307680.1:n.980-2A>T
NM_001320752.2:c.944-2A>T MANE Select	NP_001307681.2:n.944-2A>T
NM_001320753.2:c.944-2A>T	NP_001307682.1:n.944-2A>T
NM_001320754.2:c.944-2A>T	NP_001307683.1:n.944-2A>T