Canonical Allele Identifier: CA2695214247
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614375del , CM000673.2:g.57614375del GRCh38
NC_000011.9:g.57381848del , CM000673.1:g.57381848del GRCh37
NC_000011.8:g.57138424del NCBI36
NG_009625.1:g.21822del , LRG_105:g.21822del

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1297del MANE Select ENSP00000278407.4:p.Asp433ThrfsTer17
ENST00000528996.2:c.*194del ENSP00000431226.2:n.*194del
ENST00000531605.2:c.*1073del ENSP00000503752.1:n.*1073del
ENST00000619430.2:c.1093del ENSP00000478572.2:p.Asp365ThrfsTer17
ENST00000676670.1:c.1297del ENSP00000504807.1:p.Asp433ThrfsTer17
ENST00000676741.1:n.2379del
ENST00000677624.1:c.*717del ENSP00000503979.1:n.*717del
ENST00000677625.1:c.1243del ENSP00000502857.1:p.Asp415ThrfsTer17
ENST00000677856.1:n.1550del
ENST00000677915.1:c.*194del ENSP00000503118.1:n.*194del
ENST00000678533.1:c.*851del ENSP00000503873.1:n.*851del
ENST00000678592.1:c.*237del ENSP00000504424.1:n.*237del
ENST00000278407.8:c.1297del ENSP00000278407.4:p.Asp433ThrfsTer17
ENST00000340687.10:c.1186del ENSP00000341861.6:p.Asp396ThrfsTer17
ENST00000378323.8:c.1312del ENSP00000367574.4:p.Asp438ThrfsTer17
ENST00000378324.6:c.1141del ENSP00000367575.2:p.Asp381ThrfsTer17
ENST00000403558.1:c.1426del ENSP00000384420.1:p.Asp476ThrfsTer17
ENST00000528996.1:c.498del ENSP00000431226.1:n.498del
ENST00000530113.1:n.754del
ENST00000531133.5:c.798del ENSP00000435431.1:n.798del
ENST00000531797.5:c.*322del ENSP00000432554.1:n.*322del
ENST00000619430.1:c.428del ENSP00000478572.1:n.428del
NM_000062.2:c.1297del , LRG_105t1:c.1297del NP_000053.2:p.Asp433ThrfsTer17
NM_001032295.1:c.1297del NP_001027466.1:p.Asp433ThrfsTer17
NM_000062.3:c.1297del MANE Select NP_000053.2:p.Asp433ThrfsTer17
NM_001032295.2:c.1297del NP_001027466.1:p.Asp433ThrfsTer17