Canonical Allele Identifier: CA938334665
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs1945519996

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614685_57614687del , CM000673.2:g.57614685_57614687del GRCh38
NC_000011.9:g.57382158_57382160del , CM000673.1:g.57382158_57382160del GRCh37
NC_000011.8:g.57138734_57138736del NCBI36
NG_009625.1:g.22132_22134del , LRG_105:g.22132_22134del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*104_*106del MANE Select ENSP00000278407.4:n.*104_*106del
ENST00000528996.2:c.*504_*506del ENSP00000431226.2:n.*504_*506del
ENST00000531605.2:c.*1383_*1385del ENSP00000503752.1:n.*1383_*1385del
ENST00000619430.2:c.*104_*106del ENSP00000478572.2:n.*104_*106del
ENST00000676670.1:c.*15+89_*15+91del ENSP00000504807.1:n.*15+89_*15+91del
ENST00000676741.1:n.2689_2691del
ENST00000677624.1:c.*1027_*1029del ENSP00000503979.1:n.*1027_*1029del
ENST00000677625.1:c.*104_*106del ENSP00000502857.1:n.*104_*106del
ENST00000677856.1:n.1860_1862del
ENST00000677915.1:c.*504_*506del ENSP00000503118.1:n.*504_*506del
ENST00000678533.1:c.*1072+89_*1072+91del ENSP00000503873.1:n.*1072+89_*1072+91del
ENST00000678592.1:c.*547_*549del ENSP00000504424.1:n.*547_*549del
ENST00000278407.8:c.*104_*106del ENSP00000278407.4:n.*104_*106del
ENST00000340687.10:c.*104_*106del ENSP00000341861.6:n.*104_*106del
ENST00000378323.8:c.*104_*106del ENSP00000367574.4:n.*104_*106del
ENST00000378324.6:c.*104_*106del ENSP00000367575.2:n.*104_*106del
ENST00000403558.1:c.*104_*106del ENSP00000384420.1:n.*104_*106del
ENST00000528996.1:c.808_810del ENSP00000431226.1:n.808_810del
ENST00000531797.5:c.*632_*634del ENSP00000432554.1:n.*632_*634del
NM_000062.2:c.*104_*106del , LRG_105t1:c.*104_*106del NP_000053.2:n.*104_*106del
NM_001032295.1:c.*104_*106del NP_001027466.1:n.*104_*106del
NM_000062.3:c.*104_*106del MANE Select NP_000053.2:n.*104_*106del
NM_001032295.2:c.*104_*106del NP_001027466.1:n.*104_*106del