Canonical Allele Identifier: CA1975537253
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611962_57611963delinsTC , CM000673.2:g.57611962_57611963delinsTC GRCh38
NC_000011.9:g.57379435_57379436delinsTC , CM000673.1:g.57379435_57379436delinsTC GRCh37
NC_000011.8:g.57136011_57136012delinsTC NCBI36
NG_009625.1:g.19409_19410delinsTC , LRG_105:g.19409_19410delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1249+26_1249+27delinsTC MANE Select ENSP00000278407.4:n.1249+26_1249+27delinsTC
ENST00000528996.2:c.*146+26_*146+27delinsTC ENSP00000431226.2:n.*146+26_*146+27delinsTC
ENST00000531605.2:c.*1025+26_*1025+27delinsTC ENSP00000503752.1:n.*1025+26_*1025+27delinsTC
ENST00000619430.2:c.1045+26_1045+27delinsTC ENSP00000478572.2:n.1045+26_1045+27delinsTC
ENST00000676670.1:c.1249+26_1249+27delinsTC ENSP00000504807.1:n.1249+26_1249+27delinsTC
ENST00000676741.1:n.2331+26_2331+27delinsTC
ENST00000677624.1:c.*669+26_*669+27delinsTC ENSP00000503979.1:n.*669+26_*669+27delinsTC
ENST00000677625.1:c.1195+26_1195+27delinsTC ENSP00000502857.1:n.1195+26_1195+27delinsTC
ENST00000677856.1:n.1502+26_1502+27delinsTC
ENST00000677915.1:c.*146+26_*146+27delinsTC ENSP00000503118.1:n.*146+26_*146+27delinsTC
ENST00000678533.1:c.*803+26_*803+27delinsTC ENSP00000503873.1:n.*803+26_*803+27delinsTC
ENST00000678592.1:c.*189+26_*189+27delinsTC ENSP00000504424.1:n.*189+26_*189+27delinsTC
ENST00000278407.8:c.1249+26_1249+27delinsTC ENSP00000278407.4:n.1249+26_1249+27delinsTC
ENST00000340687.10:c.1138+26_1138+27delinsTC ENSP00000341861.6:n.1138+26_1138+27delinsTC
ENST00000378323.8:c.1264+26_1264+27delinsTC ENSP00000367574.4:n.1264+26_1264+27delinsTC
ENST00000378324.6:c.1093+26_1093+27delinsTC ENSP00000367575.2:n.1093+26_1093+27delinsTC
ENST00000403558.1:c.1378+26_1378+27delinsTC ENSP00000384420.1:n.1378+26_1378+27delinsTC
ENST00000528996.1:c.450+26_450+27delinsTC ENSP00000431226.1:n.450+26_450+27delinsTC
ENST00000530113.1:n.706+26_706+27delinsTC
ENST00000531133.5:c.750+26_750+27delinsTC ENSP00000435431.1:n.750+26_750+27delinsTC
ENST00000531797.5:c.*274+26_*274+27delinsTC ENSP00000432554.1:n.*274+26_*274+27delinsTC
ENST00000619430.1:c.380+26_380+27delinsTC ENSP00000478572.1:n.380+26_380+27delinsTC
NM_000062.2:c.1249+26_1249+27delinsTC , LRG_105t1:c.1249+26_1249+27delinsTC NP_000053.2:n.1249+26_1249+27delinsTC
NM_001032295.1:c.1249+26_1249+27delinsTC NP_001027466.1:n.1249+26_1249+27delinsTC
NM_000062.3:c.1249+26_1249+27delinsTC MANE Select NP_000053.2:n.1249+26_1249+27delinsTC
NM_001032295.2:c.1249+26_1249+27delinsTC NP_001027466.1:n.1249+26_1249+27delinsTC