Canonical Allele Identifier: CA1975539193
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614446G= , CM000673.2:g.57614446G= GRCh38
NC_000011.9:g.57381919G= , CM000673.1:g.57381919G= GRCh37
NC_000011.8:g.57138495G= NCBI36
NG_009625.1:g.21893G= , LRG_105:g.21893G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1368G= MANE Select ENSP00000278407.4:p.Ala456=
ENST00000528996.2:c.*265G= ENSP00000431226.2:n.*265G=
ENST00000531605.2:c.*1144G= ENSP00000503752.1:n.*1144G=
ENST00000619430.2:c.1164G= ENSP00000478572.2:p.Ala388=
ENST00000676670.1:c.1368G= ENSP00000504807.1:p.Ala456=
ENST00000676741.1:n.2450G=
ENST00000677624.1:c.*788G= ENSP00000503979.1:n.*788G=
ENST00000677625.1:c.1314G= ENSP00000502857.1:p.Ala438=
ENST00000677856.1:n.1621G=
ENST00000677915.1:c.*265G= ENSP00000503118.1:n.*265G=
ENST00000678533.1:c.*922G= ENSP00000503873.1:n.*922G=
ENST00000678592.1:c.*308G= ENSP00000504424.1:n.*308G=
ENST00000278407.8:c.1368G= ENSP00000278407.4:p.Ala456=
ENST00000340687.10:c.1257G= ENSP00000341861.6:p.Ala419=
ENST00000378323.8:c.1383G= ENSP00000367574.4:p.Ala461=
ENST00000378324.6:c.1212G= ENSP00000367575.2:p.Ala404=
ENST00000403558.1:c.1497G= ENSP00000384420.1:p.Ala499=
ENST00000528996.1:c.569G= ENSP00000431226.1:n.569G=
ENST00000530113.1:n.825G=
ENST00000531133.5:c.869G= ENSP00000435431.1:n.869G=
ENST00000531797.5:c.*393G= ENSP00000432554.1:n.*393G=
ENST00000619430.1:c.499G= ENSP00000478572.1:n.499G=
NM_000062.2:c.1368G= , LRG_105t1:c.1368G= NP_000053.2:p.Ala456=
NM_001032295.1:c.1368G= NP_001027466.1:p.Ala456=
NM_000062.3:c.1368G= MANE Select NP_000053.2:p.Ala456=
NM_001032295.2:c.1368G= NP_001027466.1:p.Ala456=