Canonical Allele Identifier: CA412021668

Gene: STS

Linked Data

• MyVariant Identifiers: chrX:g.7223087G>C (hg19) ; chrX:g.7305046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7305046G>C , CM000685.2:g.7305046G>C	GRCh38
NC_000023.10:g.7223087G>C , CM000685.1:g.7223087G>C	GRCh37
NC_000023.9:g.7233087G>C	NCBI36
NG_021472.1:g.90616G>C
NG_021472.2:g.162795G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000217961.5:c.944G>C	ENSP00000217961.5:p.Gly315Ala
ENST00000658154.1:n.1184G>C
ENST00000660000.2:c.944-20293G>C	ENSP00000499642.2:n.944-20293G>C
ENST00000664306.2:c.944G>C	ENSP00000499549.2:p.Gly315Ala
ENST00000666110.2:c.944G>C	ENSP00000499472.2:p.Gly315Ala
ENST00000674429.1:c.944G>C MANE Select	ENSP00000501534.1:p.Gly315Ala
ENST00000674499.1:c.959G>C	ENSP00000501360.1:p.Gly320Ala
ENST00000217961.4:c.959G>C	ENSP00000217961.4:p.Gly320Ala
NM_000351.4:c.959G>C	NP_000342.2:p.Gly320Ala
XM_005274511.1:c.980G>C	XP_005274568.1:p.Gly327Ala
XM_011545515.1:c.980G>C	XP_011543817.1:p.Gly327Ala
XM_011545516.1:c.980G>C	XP_011543818.1:p.Gly327Ala
XM_011545517.1:c.944G>C	XP_011543819.1:p.Gly315Ala
XM_011545518.1:c.944G>C	XP_011543820.1:p.Gly315Ala
NM_000351.5:c.959G>C	NP_000342.2:p.Gly320Ala
NM_001320750.1:c.980G>C	NP_001307679.1:p.Gly327Ala
NM_001320751.1:c.980G>C	NP_001307680.1:p.Gly327Ala
NM_001320752.1:c.980G>C	NP_001307681.1:p.Gly327Ala
NM_001320753.1:c.944G>C	NP_001307682.1:p.Gly315Ala
NM_001320754.1:c.944G>C	NP_001307683.1:p.Gly315Ala
NM_000351.7:c.944G>C	NP_000342.3:p.Gly315Ala
NM_001320750.3:c.980G>C	NP_001307679.1:p.Gly327Ala
NM_001320751.2:c.980G>C	NP_001307680.1:p.Gly327Ala
NM_001320752.2:c.944G>C MANE Select	NP_001307681.2:p.Gly315Ala
NM_001320753.2:c.944G>C	NP_001307682.1:p.Gly315Ala
NM_001320754.2:c.944G>C	NP_001307683.1:p.Gly315Ala