Canonical Allele Identifier: CA1975539262
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614482G= , CM000673.2:g.57614482G= GRCh38
NC_000011.9:g.57381955G= , CM000673.1:g.57381955G= GRCh37
NC_000011.8:g.57138531G= NCBI36
NG_009625.1:g.21929G= , LRG_105:g.21929G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1404G= MANE Select ENSP00000278407.4:p.Leu468=
ENST00000528996.2:c.*301G= ENSP00000431226.2:n.*301G=
ENST00000531605.2:c.*1180G= ENSP00000503752.1:n.*1180G=
ENST00000619430.2:c.1200G= ENSP00000478572.2:p.Leu400=
ENST00000676670.1:c.1404G= ENSP00000504807.1:p.Leu468=
ENST00000676741.1:n.2486G=
ENST00000677624.1:c.*824G= ENSP00000503979.1:n.*824G=
ENST00000677625.1:c.1350G= ENSP00000502857.1:p.Leu450=
ENST00000677856.1:n.1657G=
ENST00000677915.1:c.*301G= ENSP00000503118.1:n.*301G=
ENST00000678533.1:c.*958G= ENSP00000503873.1:n.*958G=
ENST00000678592.1:c.*344G= ENSP00000504424.1:n.*344G=
ENST00000278407.8:c.1404G= ENSP00000278407.4:p.Leu468=
ENST00000340687.10:c.1293G= ENSP00000341861.6:p.Leu431=
ENST00000378323.8:c.1419G= ENSP00000367574.4:p.Leu473=
ENST00000378324.6:c.1248G= ENSP00000367575.2:p.Leu416=
ENST00000403558.1:c.1533G= ENSP00000384420.1:p.Leu511=
ENST00000528996.1:c.605G= ENSP00000431226.1:n.605G=
ENST00000530113.1:n.861G=
ENST00000531133.5:c.905G= ENSP00000435431.1:n.905G=
ENST00000531797.5:c.*429G= ENSP00000432554.1:n.*429G=
ENST00000619430.1:c.535G= ENSP00000478572.1:n.535G=
NM_000062.2:c.1404G= , LRG_105t1:c.1404G= NP_000053.2:p.Leu468=
NM_001032295.1:c.1404G= NP_001027466.1:p.Leu468=
NM_000062.3:c.1404G= MANE Select NP_000053.2:p.Leu468=
NM_001032295.2:c.1404G= NP_001027466.1:p.Leu468=