Canonical Allele Identifier: CA918888769
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1565169693

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600257del , CM000673.2:g.57600257del GRCh38
NC_000011.9:g.57367730del , CM000673.1:g.57367730del GRCh37
NC_000011.8:g.57124306del NCBI36
NG_009625.1:g.7704del , LRG_105:g.7704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.430del MANE Select ENSP00000278407.4:p.Asp144MetfsTer4
ENST00000528996.2:c.58+1929del ENSP00000431226.2:n.58+1929del
ENST00000531605.2:c.52-1778del ENSP00000503752.1:n.52-1778del
ENST00000619430.2:c.430del ENSP00000478572.2:p.Asp144MetfsTer4
ENST00000676670.1:c.430del ENSP00000504807.1:p.Asp144MetfsTer4
ENST00000676741.1:n.1512del
ENST00000677275.1:n.417del
ENST00000677624.1:c.430del ENSP00000503979.1:p.Asp144MetfsTer4
ENST00000677625.1:c.430del ENSP00000502857.1:p.Asp144MetfsTer4
ENST00000677856.1:n.489del
ENST00000677915.1:c.430del ENSP00000503118.1:p.Asp144MetfsTer4
ENST00000678533.1:c.52-1778del ENSP00000503873.1:n.52-1778del
ENST00000678592.1:c.430del ENSP00000504424.1:p.Asp144MetfsTer4
ENST00000278407.8:c.430del ENSP00000278407.4:p.Asp144MetfsTer4
ENST00000340687.10:c.430del ENSP00000341861.6:p.Asp144MetfsTer4
ENST00000378323.8:c.445del ENSP00000367574.4:p.Asp149MetfsTer4
ENST00000378324.6:c.274del ENSP00000367575.2:p.Asp92MetfsTer4
ENST00000403558.1:c.532del ENSP00000384420.1:p.Asp178MetfsTer4
ENST00000405496.5:c.430del ENSP00000384561.1:p.Asp144MetfsTer4
ENST00000531133.5:c.52-1778del ENSP00000435431.1:n.52-1778del
ENST00000531797.5:c.52-1778del ENSP00000432554.1:n.52-1778del
ENST00000619430.1:c.348+82del ENSP00000478572.1:n.348+82del
NM_000062.2:c.430del , LRG_105t1:c.430del NP_000053.2:p.Asp144MetfsTer4
NM_001032295.1:c.430del NP_001027466.1:p.Asp144MetfsTer4
NM_000062.3:c.430del MANE Select NP_000053.2:p.Asp144MetfsTer4
NM_001032295.2:c.430del NP_001027466.1:p.Asp144MetfsTer4