Canonical Allele Identifier: CA116523
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3948
dbSNP Id: rs28940870

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614474C>A , CM000673.2:g.57614474C>A GRCh38
NC_000011.9:g.57381947C>A , CM000673.1:g.57381947C>A GRCh37
NC_000011.8:g.57138523C>A NCBI36
NG_009625.1:g.21921C>A , LRG_105:g.21921C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1396C>A MANE Select ENSP00000278407.4:p.Arg466Ser
ENST00000528996.2:c.*293C>A ENSP00000431226.2:n.*293C>A
ENST00000531605.2:c.*1172C>A ENSP00000503752.1:n.*1172C>A
ENST00000619430.2:c.1192C>A ENSP00000478572.2:p.Arg398Ser
ENST00000676670.1:c.1396C>A ENSP00000504807.1:p.Arg466Ser
ENST00000676741.1:n.2478C>A
ENST00000677624.1:c.*816C>A ENSP00000503979.1:n.*816C>A
ENST00000677625.1:c.1342C>A ENSP00000502857.1:p.Arg448Ser
ENST00000677856.1:n.1649C>A
ENST00000677915.1:c.*293C>A ENSP00000503118.1:n.*293C>A
ENST00000678533.1:c.*950C>A ENSP00000503873.1:n.*950C>A
ENST00000678592.1:c.*336C>A ENSP00000504424.1:n.*336C>A
ENST00000278407.8:c.1396C>A ENSP00000278407.4:p.Arg466Ser
ENST00000340687.10:c.1285C>A ENSP00000341861.6:p.Arg429Ser
ENST00000378323.8:c.1411C>A ENSP00000367574.4:p.Arg471Ser
ENST00000378324.6:c.1240C>A ENSP00000367575.2:p.Arg414Ser
ENST00000403558.1:c.1525C>A ENSP00000384420.1:p.Arg509Ser
ENST00000528996.1:c.597C>A ENSP00000431226.1:n.597C>A
ENST00000530113.1:n.853C>A
ENST00000531133.5:c.897C>A ENSP00000435431.1:n.897C>A
ENST00000531797.5:c.*421C>A ENSP00000432554.1:n.*421C>A
ENST00000619430.1:c.527C>A ENSP00000478572.1:n.527C>A
NM_000062.2:c.1396C>A , LRG_105t1:c.1396C>A NP_000053.2:p.Arg466Ser
NM_001032295.1:c.1396C>A NP_001027466.1:p.Arg466Ser
NM_000062.3:c.1396C>A MANE Select NP_000053.2:p.Arg466Ser
NM_001032295.2:c.1396C>A NP_001027466.1:p.Arg466Ser