Canonical Allele Identifier: CA1975539433

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614639_57614647delinsAGCCCTGCT , CM000673.2:g.57614639_57614647delinsAGCCCTGCT	GRCh38
NC_000011.9:g.57382112_57382120delinsAGCCCTGCT , CM000673.1:g.57382112_57382120delinsAGCCCTGCT	GRCh37
NC_000011.8:g.57138688_57138696delinsAGCCCTGCT	NCBI36
NG_009625.1:g.22086_22094delinsAGCCCTGCT , LRG_105:g.22086_22094delinsAGCCCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*58_*66delinsAGCCCTGCT MANE Select	ENSP00000278407.4:n.*58_*66delinsAGCCCTGCT
ENST00000528996.2:c.*458_*466delinsAGCCCTGCT	ENSP00000431226.2:n.*458_*466delinsAGCCCTGCT
ENST00000531605.2:c.*1337_*1345delinsAGCCCTGCT	ENSP00000503752.1:n.*1337_*1345delinsAGCCCTGCT
ENST00000619430.2:c.*58_*66delinsAGCCCTGCT	ENSP00000478572.2:n.*58_*66delinsAGCCCTGCT
ENST00000676670.1:c.*15+43_*15+51delinsAGCCCTGCT	ENSP00000504807.1:n.*15+43_*15+51delinsAGCCCTGCT
ENST00000676741.1:n.2643_2651delinsAGCCCTGCT
ENST00000677624.1:c.*981_*989delinsAGCCCTGCT	ENSP00000503979.1:n.*981_*989delinsAGCCCTGCT
ENST00000677625.1:c.*58_*66delinsAGCCCTGCT	ENSP00000502857.1:n.*58_*66delinsAGCCCTGCT
ENST00000677856.1:n.1814_1822delinsAGCCCTGCT
ENST00000677915.1:c.*458_*466delinsAGCCCTGCT	ENSP00000503118.1:n.*458_*466delinsAGCCCTGCT
ENST00000678533.1:c.*1072+43_*1072+51delinsAGCCCTGCT	ENSP00000503873.1:n.*1072+43_*1072+51delinsAGCCCTGCT
ENST00000678592.1:c.*501_*509delinsAGCCCTGCT	ENSP00000504424.1:n.*501_*509delinsAGCCCTGCT
ENST00000278407.8:c.*58_*66delinsAGCCCTGCT	ENSP00000278407.4:n.*58_*66delinsAGCCCTGCT
ENST00000340687.10:c.*58_*66delinsAGCCCTGCT	ENSP00000341861.6:n.*58_*66delinsAGCCCTGCT
ENST00000378323.8:c.*58_*66delinsAGCCCTGCT	ENSP00000367574.4:n.*58_*66delinsAGCCCTGCT
ENST00000378324.6:c.*58_*66delinsAGCCCTGCT	ENSP00000367575.2:n.*58_*66delinsAGCCCTGCT
ENST00000403558.1:c.*58_*66delinsAGCCCTGCT	ENSP00000384420.1:n.*58_*66delinsAGCCCTGCT
ENST00000528996.1:c.762_770delinsAGCCCTGCT	ENSP00000431226.1:n.762_770delinsAGCCCTGCT
ENST00000531797.5:c.*586_*594delinsAGCCCTGCT	ENSP00000432554.1:n.*586_*594delinsAGCCCTGCT
NM_000062.2:c.*58_*66delinsAGCCCTGCT , LRG_105t1:c.*58_*66delinsAGCCCTGCT	NP_000053.2:n.*58_*66delinsAGCCCTGCT
NM_001032295.1:c.*58_*66delinsAGCCCTGCT	NP_001027466.1:n.*58_*66delinsAGCCCTGCT
NM_000062.3:c.*58_*66delinsAGCCCTGCT MANE Select	NP_000053.2:n.*58_*66delinsAGCCCTGCT
NM_001032295.2:c.*58_*66delinsAGCCCTGCT	NP_001027466.1:n.*58_*66delinsAGCCCTGCT