Canonical Allele Identifier: CA2574828309
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614655del , CM000673.2:g.57614655del GRCh38
NC_000011.9:g.57382128del , CM000673.1:g.57382128del GRCh37
NC_000011.8:g.57138704del NCBI36
NG_009625.1:g.22102del , LRG_105:g.22102del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*74del MANE Select ENSP00000278407.4:n.*74del
ENST00000528996.2:c.*474del ENSP00000431226.2:n.*474del
ENST00000531605.2:c.*1353del ENSP00000503752.1:n.*1353del
ENST00000619430.2:c.*74del ENSP00000478572.2:n.*74del
ENST00000676670.1:c.*15+59del ENSP00000504807.1:n.*15+59del
ENST00000676741.1:n.2659del
ENST00000677624.1:c.*997del ENSP00000503979.1:n.*997del
ENST00000677625.1:c.*74del ENSP00000502857.1:n.*74del
ENST00000677856.1:n.1830del
ENST00000677915.1:c.*474del ENSP00000503118.1:n.*474del
ENST00000678533.1:c.*1072+59del ENSP00000503873.1:n.*1072+59del
ENST00000678592.1:c.*517del ENSP00000504424.1:n.*517del
ENST00000278407.8:c.*74del ENSP00000278407.4:n.*74del
ENST00000340687.10:c.*74del ENSP00000341861.6:n.*74del
ENST00000378323.8:c.*74del ENSP00000367574.4:n.*74del
ENST00000378324.6:c.*74del ENSP00000367575.2:n.*74del
ENST00000403558.1:c.*74del ENSP00000384420.1:n.*74del
ENST00000528996.1:c.778del ENSP00000431226.1:n.778del
ENST00000531797.5:c.*602del ENSP00000432554.1:n.*602del
NM_000062.2:c.*74del , LRG_105t1:c.*74del NP_000053.2:n.*74del
NM_001032295.1:c.*74del NP_001027466.1:n.*74del
NM_000062.3:c.*74del MANE Select NP_000053.2:n.*74del
NM_001032295.2:c.*74del NP_001027466.1:n.*74del