Canonical Allele Identifier: CA2739270451
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2837525
ClinVar RCV Id: RCV003692598

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614442_57614453del , CM000673.2:g.57614442_57614453del GRCh38
NC_000011.9:g.57381915_57381926del , CM000673.1:g.57381915_57381926del GRCh37
NC_000011.8:g.57138491_57138502del NCBI36
NG_009625.1:g.21889_21900del , LRG_105:g.21889_21900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1364_1375del MANE Select ENSP00000278407.4:p.Glu455_Ala458del
ENST00000528996.2:c.*261_*272del ENSP00000431226.2:n.*261_*272del
ENST00000531605.2:c.*1140_*1151del ENSP00000503752.1:n.*1140_*1151del
ENST00000619430.2:c.1160_1171del ENSP00000478572.2:p.Glu387_Ala390del
ENST00000676670.1:c.1364_1375del ENSP00000504807.1:p.Glu455_Ala458del
ENST00000676741.1:n.2446_2457del
ENST00000677624.1:c.*784_*795del ENSP00000503979.1:n.*784_*795del
ENST00000677625.1:c.1310_1321del ENSP00000502857.1:p.Glu437_Ala440del
ENST00000677856.1:n.1617_1628del
ENST00000677915.1:c.*261_*272del ENSP00000503118.1:n.*261_*272del
ENST00000678533.1:c.*918_*929del ENSP00000503873.1:n.*918_*929del
ENST00000678592.1:c.*304_*315del ENSP00000504424.1:n.*304_*315del
ENST00000278407.8:c.1364_1375del ENSP00000278407.4:p.Glu455_Ala458del
ENST00000340687.10:c.1253_1264del ENSP00000341861.6:p.Glu418_Ala421del
ENST00000378323.8:c.1379_1390del ENSP00000367574.4:p.Glu460_Ala463del
ENST00000378324.6:c.1208_1219del ENSP00000367575.2:p.Glu403_Ala406del
ENST00000403558.1:c.1493_1504del ENSP00000384420.1:p.Glu498_Ala501del
ENST00000528996.1:c.565_576del ENSP00000431226.1:n.565_576del
ENST00000530113.1:n.821_832del
ENST00000531133.5:c.865_876del ENSP00000435431.1:n.865_876del
ENST00000531797.5:c.*389_*400del ENSP00000432554.1:n.*389_*400del
ENST00000619430.1:c.495_506del ENSP00000478572.1:n.495_506del
NM_000062.2:c.1364_1375del , LRG_105t1:c.1364_1375del NP_000053.2:p.Glu455_Ala458del
NM_001032295.1:c.1364_1375del NP_001027466.1:p.Glu455_Ala458del
NM_000062.3:c.1364_1375del MANE Select NP_000053.2:p.Glu455_Ala458del
NM_001032295.2:c.1364_1375del NP_001027466.1:p.Glu455_Ala458del