Canonical Allele Identifier: CA1975539186
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614443G= , CM000673.2:g.57614443G= GRCh38
NC_000011.9:g.57381916G= , CM000673.1:g.57381916G= GRCh37
NC_000011.8:g.57138492G= NCBI36
NG_009625.1:g.21890G= , LRG_105:g.21890G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1365G= MANE Select ENSP00000278407.4:p.Glu455=
ENST00000528996.2:c.*262G= ENSP00000431226.2:n.*262G=
ENST00000531605.2:c.*1141G= ENSP00000503752.1:n.*1141G=
ENST00000619430.2:c.1161G= ENSP00000478572.2:p.Glu387=
ENST00000676670.1:c.1365G= ENSP00000504807.1:p.Glu455=
ENST00000676741.1:n.2447G=
ENST00000677624.1:c.*785G= ENSP00000503979.1:n.*785G=
ENST00000677625.1:c.1311G= ENSP00000502857.1:p.Glu437=
ENST00000677856.1:n.1618G=
ENST00000677915.1:c.*262G= ENSP00000503118.1:n.*262G=
ENST00000678533.1:c.*919G= ENSP00000503873.1:n.*919G=
ENST00000678592.1:c.*305G= ENSP00000504424.1:n.*305G=
ENST00000278407.8:c.1365G= ENSP00000278407.4:p.Glu455=
ENST00000340687.10:c.1254G= ENSP00000341861.6:p.Glu418=
ENST00000378323.8:c.1380G= ENSP00000367574.4:p.Glu460=
ENST00000378324.6:c.1209G= ENSP00000367575.2:p.Glu403=
ENST00000403558.1:c.1494G= ENSP00000384420.1:p.Glu498=
ENST00000528996.1:c.566G= ENSP00000431226.1:n.566G=
ENST00000530113.1:n.822G=
ENST00000531133.5:c.866G= ENSP00000435431.1:n.866G=
ENST00000531797.5:c.*390G= ENSP00000432554.1:n.*390G=
ENST00000619430.1:c.496G= ENSP00000478572.1:n.496G=
NM_000062.2:c.1365G= , LRG_105t1:c.1365G= NP_000053.2:p.Glu455=
NM_001032295.1:c.1365G= NP_001027466.1:p.Glu455=
NM_000062.3:c.1365G= MANE Select NP_000053.2:p.Glu455=
NM_001032295.2:c.1365G= NP_001027466.1:p.Glu455=