Canonical Allele Identifier: CA1975539246
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614475G= , CM000673.2:g.57614475G= GRCh38
NC_000011.9:g.57381948G= , CM000673.1:g.57381948G= GRCh37
NC_000011.8:g.57138524G= NCBI36
NG_009625.1:g.21922G= , LRG_105:g.21922G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1397G= MANE Select ENSP00000278407.4:p.Arg466=
ENST00000528996.2:c.*294G= ENSP00000431226.2:n.*294G=
ENST00000531605.2:c.*1173G= ENSP00000503752.1:n.*1173G=
ENST00000619430.2:c.1193G= ENSP00000478572.2:p.Arg398=
ENST00000676670.1:c.1397G= ENSP00000504807.1:p.Arg466=
ENST00000676741.1:n.2479G=
ENST00000677624.1:c.*817G= ENSP00000503979.1:n.*817G=
ENST00000677625.1:c.1343G= ENSP00000502857.1:p.Arg448=
ENST00000677856.1:n.1650G=
ENST00000677915.1:c.*294G= ENSP00000503118.1:n.*294G=
ENST00000678533.1:c.*951G= ENSP00000503873.1:n.*951G=
ENST00000678592.1:c.*337G= ENSP00000504424.1:n.*337G=
ENST00000278407.8:c.1397G= ENSP00000278407.4:p.Arg466=
ENST00000340687.10:c.1286G= ENSP00000341861.6:p.Arg429=
ENST00000378323.8:c.1412G= ENSP00000367574.4:p.Arg471=
ENST00000378324.6:c.1241G= ENSP00000367575.2:p.Arg414=
ENST00000403558.1:c.1526G= ENSP00000384420.1:p.Arg509=
ENST00000528996.1:c.598G= ENSP00000431226.1:n.598G=
ENST00000530113.1:n.854G=
ENST00000531133.5:c.898G= ENSP00000435431.1:n.898G=
ENST00000531797.5:c.*422G= ENSP00000432554.1:n.*422G=
ENST00000619430.1:c.528G= ENSP00000478572.1:n.528G=
NM_000062.2:c.1397G= , LRG_105t1:c.1397G= NP_000053.2:p.Arg466=
NM_001032295.1:c.1397G= NP_001027466.1:p.Arg466=
NM_000062.3:c.1397G= MANE Select NP_000053.2:p.Arg466=
NM_001032295.2:c.1397G= NP_001027466.1:p.Arg466=