Canonical Allele Identifier: CA2613601020

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600023-C-CCGACAACCAACT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600025_57600036dup , CM000673.2:g.57600025_57600036dup	GRCh38
NC_000011.9:g.57367498_57367509dup , CM000673.1:g.57367498_57367509dup	GRCh37
NC_000011.8:g.57124074_57124085dup	NCBI36
NG_009625.1:g.7472_7483dup , LRG_105:g.7472_7483dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.198_209dup MANE Select	ENSP00000278407.4:p.Ser70_Thr71insThrThrAsnSer
ENST00000528996.2:c.58+1697_58+1708dup	ENSP00000431226.2:n.58+1697_58+1708dup
ENST00000531605.2:c.51+1704_51+1715dup	ENSP00000503752.1:n.51+1704_51+1715dup
ENST00000619430.2:c.198_209dup	ENSP00000478572.2:p.Ser70_Thr71insThrThrAsnSer
ENST00000676670.1:c.198_209dup	ENSP00000504807.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000676741.1:n.1280_1291dup
ENST00000677275.1:n.185_196dup
ENST00000677624.1:c.198_209dup	ENSP00000503979.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000677625.1:c.198_209dup	ENSP00000502857.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000677856.1:n.257_268dup
ENST00000677915.1:c.198_209dup	ENSP00000503118.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000678533.1:c.51+1704_51+1715dup	ENSP00000503873.1:n.51+1704_51+1715dup
ENST00000678592.1:c.198_209dup	ENSP00000504424.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000278407.8:c.198_209dup	ENSP00000278407.4:p.Ser70_Thr71insThrThrAsnSer
ENST00000340687.10:c.198_209dup	ENSP00000341861.6:p.Ser70_Thr71insThrThrAsnSer
ENST00000378323.8:c.213_224dup	ENSP00000367574.4:p.Ser75_Thr76insThrThrAsnSer
ENST00000378324.6:c.42_53dup	ENSP00000367575.2:p.Ser18_Thr19insThrThrAsnSer
ENST00000403558.1:c.300_311dup	ENSP00000384420.1:p.Ser104_Thr105insThrThrAsnSer
ENST00000405496.5:c.198_209dup	ENSP00000384561.1:p.Ser70_Thr71insThrThrAsnSer
ENST00000457869.1:c.300_311dup	ENSP00000399746.1:p.Ser104_Thr105insThrThrAsnSer
ENST00000531133.5:c.51+1704_51+1715dup	ENSP00000435431.1:n.51+1704_51+1715dup
ENST00000531797.5:c.51+1704_51+1715dup	ENSP00000432554.1:n.51+1704_51+1715dup
ENST00000619430.1:c.198_209dup	ENSP00000478572.1:p.Ser70_Thr71insThrThrAsnSer
NM_000062.2:c.198_209dup , LRG_105t1:c.198_209dup	NP_000053.2:p.Ser70_Thr71insThrThrAsnSer
NM_001032295.1:c.198_209dup	NP_001027466.1:p.Ser70_Thr71insThrThrAsnSer
NM_000062.3:c.198_209dup MANE Select	NP_000053.2:p.Ser70_Thr71insThrThrAsnSer
NM_001032295.2:c.198_209dup	NP_001027466.1:p.Ser70_Thr71insThrThrAsnSer