Canonical Allele Identifier: CA380695164
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600170A>T , CM000673.2:g.57600170A>T GRCh38
NC_000011.9:g.57367643A>T , CM000673.1:g.57367643A>T GRCh37
NC_000011.8:g.57124219A>T NCBI36
NG_009625.1:g.7617A>T , LRG_105:g.7617A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.343A>T MANE Select ENSP00000278407.4:p.Thr115Ser
ENST00000528996.2:c.58+1842A>T ENSP00000431226.2:n.58+1842A>T
ENST00000531605.2:c.51+1849A>T ENSP00000503752.1:n.51+1849A>T
ENST00000619430.2:c.343A>T ENSP00000478572.2:p.Thr115Ser
ENST00000676670.1:c.343A>T ENSP00000504807.1:p.Thr115Ser
ENST00000676741.1:n.1425A>T
ENST00000677275.1:n.330A>T
ENST00000677624.1:c.343A>T ENSP00000503979.1:p.Thr115Ser
ENST00000677625.1:c.343A>T ENSP00000502857.1:p.Thr115Ser
ENST00000677856.1:n.402A>T
ENST00000677915.1:c.343A>T ENSP00000503118.1:p.Thr115Ser
ENST00000678533.1:c.51+1849A>T ENSP00000503873.1:n.51+1849A>T
ENST00000678592.1:c.343A>T ENSP00000504424.1:p.Thr115Ser
ENST00000278407.8:c.343A>T ENSP00000278407.4:p.Thr115Ser
ENST00000340687.10:c.343A>T ENSP00000341861.6:p.Thr115Ser
ENST00000378323.8:c.358A>T ENSP00000367574.4:p.Thr120Ser
ENST00000378324.6:c.187A>T ENSP00000367575.2:p.Thr63Ser
ENST00000403558.1:c.445A>T ENSP00000384420.1:p.Thr149Ser
ENST00000405496.5:c.343A>T ENSP00000384561.1:p.Thr115Ser
ENST00000531133.5:c.51+1849A>T ENSP00000435431.1:n.51+1849A>T
ENST00000531797.5:c.51+1849A>T ENSP00000432554.1:n.51+1849A>T
ENST00000619430.1:c.343A>T ENSP00000478572.1:p.Thr115Ser
NM_000062.2:c.343A>T , LRG_105t1:c.343A>T NP_000053.2:p.Thr115Ser
NM_001032295.1:c.343A>T NP_001027466.1:p.Thr115Ser
NM_000062.3:c.343A>T MANE Select NP_000053.2:p.Thr115Ser
NM_001032295.2:c.343A>T NP_001027466.1:p.Thr115Ser