Canonical Allele Identifier: CA380690721

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 487524
• ClinVar RCV Id: RCV000576893
• dbSNP Id: rs763451792
• MyVariant Identifiers: chr11:g.57381936T>G (hg19) ; chr11:g.57614463T>G (hg38)
• PubMed: PMID:17137866

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614463T>G , CM000673.2:g.57614463T>G	GRCh38
NC_000011.9:g.57381936T>G , CM000673.1:g.57381936T>G	GRCh37
NC_000011.8:g.57138512T>G	NCBI36
NG_009625.1:g.21910T>G , LRG_105:g.21910T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1385T>G MANE Select	ENSP00000278407.4:p.Ile462Ser
ENST00000528996.2:c.*282T>G	ENSP00000431226.2:n.*282T>G
ENST00000531605.2:c.*1161T>G	ENSP00000503752.1:n.*1161T>G
ENST00000619430.2:c.1181T>G	ENSP00000478572.2:p.Ile394Ser
ENST00000676670.1:c.1385T>G	ENSP00000504807.1:p.Ile462Ser
ENST00000676741.1:n.2467T>G
ENST00000677624.1:c.*805T>G	ENSP00000503979.1:n.*805T>G
ENST00000677625.1:c.1331T>G	ENSP00000502857.1:p.Ile444Ser
ENST00000677856.1:n.1638T>G
ENST00000677915.1:c.*282T>G	ENSP00000503118.1:n.*282T>G
ENST00000678533.1:c.*939T>G	ENSP00000503873.1:n.*939T>G
ENST00000678592.1:c.*325T>G	ENSP00000504424.1:n.*325T>G
ENST00000278407.8:c.1385T>G	ENSP00000278407.4:p.Ile462Ser
ENST00000340687.10:c.1274T>G	ENSP00000341861.6:p.Ile425Ser
ENST00000378323.8:c.1400T>G	ENSP00000367574.4:p.Ile467Ser
ENST00000378324.6:c.1229T>G	ENSP00000367575.2:p.Ile410Ser
ENST00000403558.1:c.1514T>G	ENSP00000384420.1:p.Ile505Ser
ENST00000528996.1:c.586T>G	ENSP00000431226.1:n.586T>G
ENST00000530113.1:n.842T>G
ENST00000531133.5:c.886T>G	ENSP00000435431.1:n.886T>G
ENST00000531797.5:c.*410T>G	ENSP00000432554.1:n.*410T>G
ENST00000619430.1:c.516T>G	ENSP00000478572.1:n.516T>G
NM_000062.2:c.1385T>G , LRG_105t1:c.1385T>G	NP_000053.2:p.Ile462Ser
NM_001032295.1:c.1385T>G	NP_001027466.1:p.Ile462Ser
NM_000062.3:c.1385T>G MANE Select	NP_000053.2:p.Ile462Ser
NM_001032295.2:c.1385T>G	NP_001027466.1:p.Ile462Ser