Canonical Allele Identifier: CA2837995315
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611806_57611829del , CM000673.2:g.57611806_57611829del GRCh38
NC_000011.9:g.57379279_57379302del , CM000673.1:g.57379279_57379302del GRCh37
NC_000011.8:g.57135855_57135878del NCBI36
NG_009625.1:g.19253_19276del , LRG_105:g.19253_19276del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1119_1142del MANE Select ENSP00000278407.4:p.Leu374_Ala381del
ENST00000528996.2:c.*16_*39del ENSP00000431226.2:n.*16_*39del
ENST00000531605.2:c.*895_*918del ENSP00000503752.1:n.*895_*918del
ENST00000619430.2:c.915_938del ENSP00000478572.2:p.Leu306_Ala313del
ENST00000676670.1:c.1119_1142del ENSP00000504807.1:p.Leu374_Ala381del
ENST00000676741.1:n.2201_2224del
ENST00000677624.1:c.*539_*562del ENSP00000503979.1:n.*539_*562del
ENST00000677625.1:c.1065_1088del ENSP00000502857.1:p.Leu356_Ala363del
ENST00000677856.1:n.1372_1395del
ENST00000677915.1:c.*16_*39del ENSP00000503118.1:n.*16_*39del
ENST00000678533.1:c.*673_*696del ENSP00000503873.1:n.*673_*696del
ENST00000678592.1:c.*59_*82del ENSP00000504424.1:n.*59_*82del
ENST00000278407.8:c.1119_1142del ENSP00000278407.4:p.Leu374_Ala381del
ENST00000340687.10:c.1030-22_1031del
ENST00000378323.8:c.1134_1157del ENSP00000367574.4:p.Leu379_Ala386del
ENST00000378324.6:c.963_986del ENSP00000367575.2:p.Leu322_Ala329del
ENST00000403558.1:c.1248_1271del ENSP00000384420.1:p.Leu417_Ala424del
ENST00000528996.1:c.320_343del ENSP00000431226.1:n.320_343del
ENST00000530113.1:n.576_599del
ENST00000531133.5:c.620_643del ENSP00000435431.1:n.620_643del
ENST00000531797.5:c.*144_*167del ENSP00000432554.1:n.*144_*167del
ENST00000619430.1:c.349-99_349-76del ENSP00000478572.1:n.349-99_349-76del
NM_000062.2:c.1119_1142del , LRG_105t1:c.1119_1142del NP_000053.2:p.Leu374_Ala381del
NM_001032295.1:c.1119_1142del NP_001027466.1:p.Leu374_Ala381del
NM_000062.3:c.1119_1142del MANE Select NP_000053.2:p.Leu374_Ala381del
NM_001032295.2:c.1119_1142del NP_001027466.1:p.Leu374_Ala381del