Canonical Allele Identifier: CA380690843

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 2769565
• ClinVar RCV Id: RCV003578796
• MyVariant Identifiers: chr11:g.57381996G>A (hg19) ; chr11:g.57614523G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614523G>A , CM000673.2:g.57614523G>A	GRCh38
NC_000011.9:g.57381996G>A , CM000673.1:g.57381996G>A	GRCh37
NC_000011.8:g.57138572G>A	NCBI36
NG_009625.1:g.21970G>A , LRG_105:g.21970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1445G>A MANE Select	ENSP00000278407.4:p.Trp482Ter
ENST00000528996.2:c.*342G>A	ENSP00000431226.2:n.*342G>A
ENST00000531605.2:c.*1221G>A	ENSP00000503752.1:n.*1221G>A
ENST00000619430.2:c.1241G>A	ENSP00000478572.2:p.Trp414Ter
ENST00000676670.1:c.1445G>A	ENSP00000504807.1:p.Trp482Ter
ENST00000676741.1:n.2527G>A
ENST00000677624.1:c.*865G>A	ENSP00000503979.1:n.*865G>A
ENST00000677625.1:c.1391G>A	ENSP00000502857.1:p.Trp464Ter
ENST00000677856.1:n.1698G>A
ENST00000677915.1:c.*342G>A	ENSP00000503118.1:n.*342G>A
ENST00000678533.1:c.*999G>A	ENSP00000503873.1:n.*999G>A
ENST00000678592.1:c.*385G>A	ENSP00000504424.1:n.*385G>A
ENST00000278407.8:c.1445G>A	ENSP00000278407.4:p.Trp482Ter
ENST00000340687.10:c.1334G>A	ENSP00000341861.6:p.Trp445Ter
ENST00000378323.8:c.1460G>A	ENSP00000367574.4:p.Trp487Ter
ENST00000378324.6:c.1289G>A	ENSP00000367575.2:p.Trp430Ter
ENST00000403558.1:c.1574G>A	ENSP00000384420.1:p.Trp525Ter
ENST00000528996.1:c.646G>A	ENSP00000431226.1:n.646G>A
ENST00000530113.1:n.902G>A
ENST00000531133.5:c.946G>A	ENSP00000435431.1:n.946G>A
ENST00000531797.5:c.*470G>A	ENSP00000432554.1:n.*470G>A
ENST00000619430.1:c.576G>A	ENSP00000478572.1:n.576G>A
NM_000062.2:c.1445G>A , LRG_105t1:c.1445G>A	NP_000053.2:p.Trp482Ter
NM_001032295.1:c.1445G>A	NP_001027466.1:p.Trp482Ter
NM_000062.3:c.1445G>A MANE Select	NP_000053.2:p.Trp482Ter
NM_001032295.2:c.1445G>A	NP_001027466.1:p.Trp482Ter