Canonical Allele Identifier: CA1975539254
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614480C= , CM000673.2:g.57614480C= GRCh38
NC_000011.9:g.57381953C= , CM000673.1:g.57381953C= GRCh37
NC_000011.8:g.57138529C= NCBI36
NG_009625.1:g.21927C= , LRG_105:g.21927C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1402C= MANE Select ENSP00000278407.4:p.Leu468=
ENST00000528996.2:c.*299C= ENSP00000431226.2:n.*299C=
ENST00000531605.2:c.*1178C= ENSP00000503752.1:n.*1178C=
ENST00000619430.2:c.1198C= ENSP00000478572.2:p.Leu400=
ENST00000676670.1:c.1402C= ENSP00000504807.1:p.Leu468=
ENST00000676741.1:n.2484C=
ENST00000677624.1:c.*822C= ENSP00000503979.1:n.*822C=
ENST00000677625.1:c.1348C= ENSP00000502857.1:p.Leu450=
ENST00000677856.1:n.1655C=
ENST00000677915.1:c.*299C= ENSP00000503118.1:n.*299C=
ENST00000678533.1:c.*956C= ENSP00000503873.1:n.*956C=
ENST00000678592.1:c.*342C= ENSP00000504424.1:n.*342C=
ENST00000278407.8:c.1402C= ENSP00000278407.4:p.Leu468=
ENST00000340687.10:c.1291C= ENSP00000341861.6:p.Leu431=
ENST00000378323.8:c.1417C= ENSP00000367574.4:p.Leu473=
ENST00000378324.6:c.1246C= ENSP00000367575.2:p.Leu416=
ENST00000403558.1:c.1531C= ENSP00000384420.1:p.Leu511=
ENST00000528996.1:c.603C= ENSP00000431226.1:n.603C=
ENST00000530113.1:n.859C=
ENST00000531133.5:c.903C= ENSP00000435431.1:n.903C=
ENST00000531797.5:c.*427C= ENSP00000432554.1:n.*427C=
ENST00000619430.1:c.533C= ENSP00000478572.1:n.533C=
NM_000062.2:c.1402C= , LRG_105t1:c.1402C= NP_000053.2:p.Leu468=
NM_001032295.1:c.1402C= NP_001027466.1:p.Leu468=
NM_000062.3:c.1402C= MANE Select NP_000053.2:p.Leu468=
NM_001032295.2:c.1402C= NP_001027466.1:p.Leu468=