Canonical Allele Identifier: CA412021673

Gene: STS

Linked Data

• MyVariant Identifiers: chrX:g.7223090A>C (hg19) ; chrX:g.7305049A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.7305049A>C , CM000685.2:g.7305049A>C	GRCh38
NC_000023.10:g.7223090A>C , CM000685.1:g.7223090A>C	GRCh37
NC_000023.9:g.7233090A>C	NCBI36
NG_021472.1:g.90619A>C
NG_021472.2:g.162798A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000217961.5:c.947A>C	ENSP00000217961.5:p.Gln316Pro
ENST00000658154.1:n.1187A>C
ENST00000660000.2:c.944-20290A>C	ENSP00000499642.2:n.944-20290A>C
ENST00000664306.2:c.947A>C	ENSP00000499549.2:p.Gln316Pro
ENST00000666110.2:c.947A>C	ENSP00000499472.2:p.Gln316Pro
ENST00000674429.1:c.947A>C MANE Select	ENSP00000501534.1:p.Gln316Pro
ENST00000674499.1:c.962A>C	ENSP00000501360.1:p.Gln321Pro
ENST00000217961.4:c.962A>C	ENSP00000217961.4:p.Gln321Pro
NM_000351.4:c.962A>C	NP_000342.2:p.Gln321Pro
XM_005274511.1:c.983A>C	XP_005274568.1:p.Gln328Pro
XM_011545515.1:c.983A>C	XP_011543817.1:p.Gln328Pro
XM_011545516.1:c.983A>C	XP_011543818.1:p.Gln328Pro
XM_011545517.1:c.947A>C	XP_011543819.1:p.Gln316Pro
XM_011545518.1:c.947A>C	XP_011543820.1:p.Gln316Pro
NM_000351.5:c.962A>C	NP_000342.2:p.Gln321Pro
NM_001320750.1:c.983A>C	NP_001307679.1:p.Gln328Pro
NM_001320751.1:c.983A>C	NP_001307680.1:p.Gln328Pro
NM_001320752.1:c.983A>C	NP_001307681.1:p.Gln328Pro
NM_001320753.1:c.947A>C	NP_001307682.1:p.Gln316Pro
NM_001320754.1:c.947A>C	NP_001307683.1:p.Gln316Pro
NM_000351.7:c.947A>C	NP_000342.3:p.Gln316Pro
NM_001320750.3:c.983A>C	NP_001307679.1:p.Gln328Pro
NM_001320751.2:c.983A>C	NP_001307680.1:p.Gln328Pro
NM_001320752.2:c.947A>C MANE Select	NP_001307681.2:p.Gln316Pro
NM_001320753.2:c.947A>C	NP_001307682.1:p.Gln316Pro
NM_001320754.2:c.947A>C	NP_001307683.1:p.Gln316Pro