Canonical Allele Identifier: CA1975539055
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614366C= , CM000673.2:g.57614366C= GRCh38
NC_000011.9:g.57381839C= , CM000673.1:g.57381839C= GRCh37
NC_000011.8:g.57138415C= NCBI36
NG_009625.1:g.21813C= , LRG_105:g.21813C=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1288C= MANE Select ENSP00000278407.4:p.Leu430=
ENST00000528996.2:c.*185C= ENSP00000431226.2:n.*185C=
ENST00000531605.2:c.*1064C= ENSP00000503752.1:n.*1064C=
ENST00000619430.2:c.1084C= ENSP00000478572.2:p.Leu362=
ENST00000676670.1:c.1288C= ENSP00000504807.1:p.Leu430=
ENST00000676741.1:n.2370C=
ENST00000677624.1:c.*708C= ENSP00000503979.1:n.*708C=
ENST00000677625.1:c.1234C= ENSP00000502857.1:p.Leu412=
ENST00000677856.1:n.1541C=
ENST00000677915.1:c.*185C= ENSP00000503118.1:n.*185C=
ENST00000678533.1:c.*842C= ENSP00000503873.1:n.*842C=
ENST00000678592.1:c.*228C= ENSP00000504424.1:n.*228C=
ENST00000278407.8:c.1288C= ENSP00000278407.4:p.Leu430=
ENST00000340687.10:c.1177C= ENSP00000341861.6:p.Leu393=
ENST00000378323.8:c.1303C= ENSP00000367574.4:p.Leu435=
ENST00000378324.6:c.1132C= ENSP00000367575.2:p.Leu378=
ENST00000403558.1:c.1417C= ENSP00000384420.1:p.Leu473=
ENST00000528996.1:c.489C= ENSP00000431226.1:n.489C=
ENST00000530113.1:n.745C=
ENST00000531133.5:c.789C= ENSP00000435431.1:n.789C=
ENST00000531797.5:c.*313C= ENSP00000432554.1:n.*313C=
ENST00000619430.1:c.419C= ENSP00000478572.1:n.419C=
NM_000062.2:c.1288C= , LRG_105t1:c.1288C= NP_000053.2:p.Leu430=
NM_001032295.1:c.1288C= NP_001027466.1:p.Leu430=
NM_000062.3:c.1288C= MANE Select NP_000053.2:p.Leu430=
NM_001032295.2:c.1288C= NP_001027466.1:p.Leu430=