Canonical Allele Identifier: CA678625997

Gene: SERPING1

Linked Data

• dbSNP Id: rs1373884372
• gnomAD v3: 11-57599765-ACT-A
• gnomAD v4: 11-57599765-ACT-A
• MyVariant Identifiers: chr11:g.57367239_57367240del (hg19) ; chr11:g.57599766_57599767del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57599770_57599771del , CM000673.2:g.57599770_57599771del	GRCh38
NC_000011.9:g.57367243_57367244del , CM000673.1:g.57367243_57367244del	GRCh37
NC_000011.8:g.57123819_57123820del	NCBI36
NG_009625.1:g.7217_7218del , LRG_105:g.7217_7218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.52-109_52-108del MANE Select	ENSP00000278407.4:n.52-109_52-108del
ENST00000528996.2:c.58+1442_58+1443del	ENSP00000431226.2:n.58+1442_58+1443del
ENST00000531605.2:c.51+1449_51+1450del	ENSP00000503752.1:n.51+1449_51+1450del
ENST00000619430.2:c.52-109_52-108del	ENSP00000478572.2:n.52-109_52-108del
ENST00000676670.1:c.52-109_52-108del	ENSP00000504807.1:n.52-109_52-108del
ENST00000676741.1:n.1025_1026del
ENST00000677275.1:n.39-109_39-108del
ENST00000677624.1:c.52-109_52-108del	ENSP00000503979.1:n.52-109_52-108del
ENST00000677625.1:c.52-109_52-108del	ENSP00000502857.1:n.52-109_52-108del
ENST00000677856.1:n.111-109_111-108del
ENST00000677915.1:c.52-109_52-108del	ENSP00000503118.1:n.52-109_52-108del
ENST00000678533.1:c.51+1449_51+1450del	ENSP00000503873.1:n.51+1449_51+1450del
ENST00000678592.1:c.52-109_52-108del	ENSP00000504424.1:n.52-109_52-108del
ENST00000278407.8:c.52-109_52-108del	ENSP00000278407.4:n.52-109_52-108del
ENST00000340687.10:c.52-109_52-108del	ENSP00000341861.6:n.52-109_52-108del
ENST00000378323.8:c.52-94_52-93del	ENSP00000367574.4:n.52-94_52-93del
ENST00000378324.6:c.-105-109_-105-108del	ENSP00000367575.2:n.-105-109_-105-108del
ENST00000403558.1:c.154-109_154-108del	ENSP00000384420.1:n.154-109_154-108del
ENST00000405496.5:c.52-109_52-108del	ENSP00000384561.1:n.52-109_52-108del
ENST00000457869.1:c.154-109_154-108del	ENSP00000399746.1:n.154-109_154-108del
ENST00000531133.5:c.51+1449_51+1450del	ENSP00000435431.1:n.51+1449_51+1450del
ENST00000531797.5:c.51+1449_51+1450del	ENSP00000432554.1:n.51+1449_51+1450del
ENST00000619430.1:c.52-109_52-108del	ENSP00000478572.1:n.52-109_52-108del
NM_000062.2:c.52-109_52-108del , LRG_105t1:c.52-109_52-108del	NP_000053.2:n.52-109_52-108del
NM_001032295.1:c.52-109_52-108del	NP_001027466.1:n.52-109_52-108del
NM_000062.3:c.52-109_52-108del MANE Select	NP_000053.2:n.52-109_52-108del
NM_001032295.2:c.52-109_52-108del	NP_001027466.1:n.52-109_52-108del