Canonical Allele Identifier: CA1975539556
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614759A= , CM000673.2:g.57614759A= GRCh38
NC_000011.9:g.57382232A= , CM000673.1:g.57382232A= GRCh37
NC_000011.8:g.57138808A= NCBI36
NG_009625.1:g.22206A= , LRG_105:g.22206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*178A= MANE Select ENSP00000278407.4:n.*178A=
ENST00000528996.2:c.*578A= ENSP00000431226.2:n.*578A=
ENST00000531605.2:c.*1457A= ENSP00000503752.1:n.*1457A=
ENST00000619430.2:c.*178A= ENSP00000478572.2:n.*178A=
ENST00000676670.1:c.*15+163A= ENSP00000504807.1:n.*15+163A=
ENST00000676741.1:n.2763A=
ENST00000677624.1:c.*1101A= ENSP00000503979.1:n.*1101A=
ENST00000677625.1:c.*178A= ENSP00000502857.1:n.*178A=
ENST00000677856.1:n.1934A=
ENST00000677915.1:c.*578A= ENSP00000503118.1:n.*578A=
ENST00000678533.1:c.*1072+163A= ENSP00000503873.1:n.*1072+163A=
ENST00000678592.1:c.*621A= ENSP00000504424.1:n.*621A=
ENST00000278407.8:c.*178A= ENSP00000278407.4:n.*178A=
ENST00000340687.10:c.*178A= ENSP00000341861.6:n.*178A=
ENST00000378324.6:c.*178A= ENSP00000367575.2:n.*178A=
ENST00000403558.1:c.*178A= ENSP00000384420.1:n.*178A=
ENST00000528996.1:c.882A= ENSP00000431226.1:n.882A=
ENST00000531797.5:c.*706A= ENSP00000432554.1:n.*706A=
NM_000062.2:c.*178A= , LRG_105t1:c.*178A= NP_000053.2:n.*178A=
NM_001032295.1:c.*178A= NP_001027466.1:n.*178A=
NM_000062.3:c.*178A= MANE Select NP_000053.2:n.*178A=
NM_001032295.2:c.*178A= NP_001027466.1:n.*178A=