Canonical Allele Identifier: CA1975539296
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614510C= , CM000673.2:g.57614510C= GRCh38
NC_000011.9:g.57381983C= , CM000673.1:g.57381983C= GRCh37
NC_000011.8:g.57138559C= NCBI36
NG_009625.1:g.21957C= , LRG_105:g.21957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1432C= MANE Select ENSP00000278407.4:p.Leu478=
ENST00000528996.2:c.*329C= ENSP00000431226.2:n.*329C=
ENST00000531605.2:c.*1208C= ENSP00000503752.1:n.*1208C=
ENST00000619430.2:c.1228C= ENSP00000478572.2:p.Leu410=
ENST00000676670.1:c.1432C= ENSP00000504807.1:p.Leu478=
ENST00000676741.1:n.2514C=
ENST00000677624.1:c.*852C= ENSP00000503979.1:n.*852C=
ENST00000677625.1:c.1378C= ENSP00000502857.1:p.Leu460=
ENST00000677856.1:n.1685C=
ENST00000677915.1:c.*329C= ENSP00000503118.1:n.*329C=
ENST00000678533.1:c.*986C= ENSP00000503873.1:n.*986C=
ENST00000678592.1:c.*372C= ENSP00000504424.1:n.*372C=
ENST00000278407.8:c.1432C= ENSP00000278407.4:p.Leu478=
ENST00000340687.10:c.1321C= ENSP00000341861.6:p.Leu441=
ENST00000378323.8:c.1447C= ENSP00000367574.4:p.Leu483=
ENST00000378324.6:c.1276C= ENSP00000367575.2:p.Leu426=
ENST00000403558.1:c.1561C= ENSP00000384420.1:p.Leu521=
ENST00000528996.1:c.633C= ENSP00000431226.1:n.633C=
ENST00000530113.1:n.889C=
ENST00000531133.5:c.933C= ENSP00000435431.1:n.933C=
ENST00000531797.5:c.*457C= ENSP00000432554.1:n.*457C=
ENST00000619430.1:c.563C= ENSP00000478572.1:n.563C=
NM_000062.2:c.1432C= , LRG_105t1:c.1432C= NP_000053.2:p.Leu478=
NM_001032295.1:c.1432C= NP_001027466.1:p.Leu478=
NM_000062.3:c.1432C= MANE Select NP_000053.2:p.Leu478=
NM_001032295.2:c.1432C= NP_001027466.1:p.Leu478=