Canonical Allele Identifier: CA2792230152
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614714C>T , CM000673.2:g.57614714C>T GRCh38
NC_000011.9:g.57382187C>T , CM000673.1:g.57382187C>T GRCh37
NC_000011.8:g.57138763C>T NCBI36
NG_009625.1:g.22161C>T , LRG_105:g.22161C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*133C>T MANE Select ENSP00000278407.4:n.*133C>T
ENST00000528996.2:c.*533C>T ENSP00000431226.2:n.*533C>T
ENST00000531605.2:c.*1412C>T ENSP00000503752.1:n.*1412C>T
ENST00000619430.2:c.*133C>T ENSP00000478572.2:n.*133C>T
ENST00000676670.1:c.*15+118C>T ENSP00000504807.1:n.*15+118C>T
ENST00000676741.1:n.2718C>T
ENST00000677624.1:c.*1056C>T ENSP00000503979.1:n.*1056C>T
ENST00000677625.1:c.*133C>T ENSP00000502857.1:n.*133C>T
ENST00000677856.1:n.1889C>T
ENST00000677915.1:c.*533C>T ENSP00000503118.1:n.*533C>T
ENST00000678533.1:c.*1072+118C>T ENSP00000503873.1:n.*1072+118C>T
ENST00000678592.1:c.*576C>T ENSP00000504424.1:n.*576C>T
ENST00000278407.8:c.*133C>T ENSP00000278407.4:n.*133C>T
ENST00000340687.10:c.*133C>T ENSP00000341861.6:n.*133C>T
ENST00000378323.8:c.*133C>T ENSP00000367574.4:n.*133C>T
ENST00000378324.6:c.*133C>T ENSP00000367575.2:n.*133C>T
ENST00000403558.1:c.*133C>T ENSP00000384420.1:n.*133C>T
ENST00000528996.1:c.837C>T ENSP00000431226.1:n.837C>T
ENST00000531797.5:c.*661C>T ENSP00000432554.1:n.*661C>T
NM_000062.2:c.*133C>T , LRG_105t1:c.*133C>T NP_000053.2:n.*133C>T
NM_001032295.1:c.*133C>T NP_001027466.1:n.*133C>T
NM_000062.3:c.*133C>T MANE Select NP_000053.2:n.*133C>T
NM_001032295.2:c.*133C>T NP_001027466.1:n.*133C>T