Canonical Allele Identifier: CA2695214288
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614683_57614837del , CM000673.2:g.57614683_57614837del GRCh38
NC_000011.9:g.57382156_57382310del , CM000673.1:g.57382156_57382310del GRCh37
NC_000011.8:g.57138732_57138886del NCBI36
NG_009625.1:g.22130_22284del , LRG_105:g.22130_22284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*102_*256del MANE Select ENSP00000278407.4:n.*102_*256del
ENST00000528996.2:c.*502_*656del ENSP00000431226.2:n.*502_*656del
ENST00000531605.2:c.*1381_*1535del ENSP00000503752.1:n.*1381_*1535del
ENST00000619430.2:c.*102_*256del ENSP00000478572.2:n.*102_*256del
ENST00000676670.1:c.*15+87_*15+241del ENSP00000504807.1:n.*15+87_*15+241del
ENST00000676741.1:n.2687_2841del
ENST00000677624.1:c.*1025_*1179del ENSP00000503979.1:n.*1025_*1179del
ENST00000677856.1:n.1858_2012del
ENST00000678533.1:c.*1072+87_*1072+241del ENSP00000503873.1:n.*1072+87_*1072+241del
ENST00000278407.8:c.*102_*256del ENSP00000278407.4:n.*102_*256del
ENST00000340687.10:c.*102_*256del ENSP00000341861.6:n.*102_*256del
ENST00000378324.6:c.*102_*256del ENSP00000367575.2:n.*102_*256del
NM_000062.2:c.*102_*256del , LRG_105t1:c.*102_*256del NP_000053.2:n.*102_*256del
NM_001032295.1:c.*102_*256del NP_001027466.1:n.*102_*256del
NM_000062.3:c.*102_*256del MANE Select NP_000053.2:n.*102_*256del
NM_001032295.2:c.*102_*256del NP_001027466.1:n.*102_*256del