Canonical Allele Identifier: CA2597201627

Gene: SERPING1

Linked Data

• gnomAD v3: 11-57612123-CT-C
• gnomAD v4: 11-57612123-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57612126del , CM000673.2:g.57612126del	GRCh38
NC_000011.9:g.57379599del , CM000673.1:g.57379599del	GRCh37
NC_000011.8:g.57136175del	NCBI36
NG_009625.1:g.19573del , LRG_105:g.19573del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1249+190del MANE Select	ENSP00000278407.4:n.1249+190del
ENST00000528996.2:c.*146+190del	ENSP00000431226.2:n.*146+190del
ENST00000531605.2:c.*1025+190del	ENSP00000503752.1:n.*1025+190del
ENST00000619430.2:c.1045+190del	ENSP00000478572.2:n.1045+190del
ENST00000676670.1:c.1249+190del	ENSP00000504807.1:n.1249+190del
ENST00000676741.1:n.2331+190del
ENST00000677624.1:c.*669+190del	ENSP00000503979.1:n.*669+190del
ENST00000677625.1:c.1195+190del	ENSP00000502857.1:n.1195+190del
ENST00000677856.1:n.1502+190del
ENST00000677915.1:c.*146+190del	ENSP00000503118.1:n.*146+190del
ENST00000678533.1:c.*803+190del	ENSP00000503873.1:n.*803+190del
ENST00000678592.1:c.*189+190del	ENSP00000504424.1:n.*189+190del
ENST00000278407.8:c.1249+190del	ENSP00000278407.4:n.1249+190del
ENST00000340687.10:c.1138+190del	ENSP00000341861.6:n.1138+190del
ENST00000378323.8:c.1264+190del	ENSP00000367574.4:n.1264+190del
ENST00000378324.6:c.1093+190del	ENSP00000367575.2:n.1093+190del
ENST00000403558.1:c.1378+190del	ENSP00000384420.1:n.1378+190del
ENST00000528996.1:c.450+190del	ENSP00000431226.1:n.450+190del
ENST00000530113.1:n.706+190del
ENST00000531133.5:c.750+190del	ENSP00000435431.1:n.750+190del
ENST00000531797.5:c.*274+190del	ENSP00000432554.1:n.*274+190del
ENST00000619430.1:c.380+190del	ENSP00000478572.1:n.380+190del
NM_000062.2:c.1249+190del , LRG_105t1:c.1249+190del	NP_000053.2:n.1249+190del
NM_001032295.1:c.1249+190del	NP_001027466.1:n.1249+190del
NM_000062.3:c.1249+190del MANE Select	NP_000053.2:n.1249+190del
NM_001032295.2:c.1249+190del	NP_001027466.1:n.1249+190del