Canonical Allele Identifier: CA2414181920
Gene: STS HGNC NCBI

Linked Data

dbSNP Id: rs780807042
gnomAD v4: X-7305012-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.7305012C>A , CM000685.2:g.7305012C>A GRCh38
NC_000023.10:g.7223053C>A , CM000685.1:g.7223053C>A GRCh37
NC_000023.9:g.7233053C>A NCBI36
NG_021472.1:g.90582C>A
NG_021472.2:g.162761C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000217961.5:c.944-34C>A ENSP00000217961.5:n.944-34C>A
ENST00000658154.1:n.1184-34C>A
ENST00000660000.2:c.944-20327C>A ENSP00000499642.2:n.944-20327C>A
ENST00000664306.2:c.944-34C>A ENSP00000499549.2:n.944-34C>A
ENST00000666110.2:c.944-34C>A ENSP00000499472.2:n.944-34C>A
ENST00000674429.1:c.944-34C>A MANE Select ENSP00000501534.1:n.944-34C>A
ENST00000674499.1:c.959-34C>A ENSP00000501360.1:n.959-34C>A
ENST00000217961.4:c.959-34C>A ENSP00000217961.4:n.959-34C>A
NM_000351.4:c.959-34C>A NP_000342.2:n.959-34C>A
XM_005274511.1:c.980-34C>A XP_005274568.1:n.980-34C>A
XM_011545515.1:c.980-34C>A XP_011543817.1:n.980-34C>A
XM_011545516.1:c.980-34C>A XP_011543818.1:n.980-34C>A
XM_011545517.1:c.944-34C>A XP_011543819.1:n.944-34C>A
XM_011545518.1:c.944-34C>A XP_011543820.1:n.944-34C>A
NM_000351.5:c.959-34C>A NP_000342.2:n.959-34C>A
NM_001320750.1:c.980-34C>A NP_001307679.1:n.980-34C>A
NM_001320751.1:c.980-34C>A NP_001307680.1:n.980-34C>A
NM_001320752.1:c.980-34C>A NP_001307681.1:n.980-34C>A
NM_001320753.1:c.944-34C>A NP_001307682.1:n.944-34C>A
NM_001320754.1:c.944-34C>A NP_001307683.1:n.944-34C>A
NM_000351.7:c.944-34C>A NP_000342.3:n.944-34C>A
NM_001320750.3:c.980-34C>A NP_001307679.1:n.980-34C>A
NM_001320751.2:c.980-34C>A NP_001307680.1:n.980-34C>A
NM_001320752.2:c.944-34C>A MANE Select NP_001307681.2:n.944-34C>A
NM_001320753.2:c.944-34C>A NP_001307682.1:n.944-34C>A
NM_001320754.2:c.944-34C>A NP_001307683.1:n.944-34C>A