Canonical Allele Identifier: CA2613603785
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614708del , CM000673.2:g.57614708del GRCh38
NC_000011.9:g.57382181del , CM000673.1:g.57382181del GRCh37
NC_000011.8:g.57138757del NCBI36
NG_009625.1:g.22155del , LRG_105:g.22155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.*127del MANE Select ENSP00000278407.4:n.*127del
ENST00000528996.2:c.*527del ENSP00000431226.2:n.*527del
ENST00000531605.2:c.*1406del ENSP00000503752.1:n.*1406del
ENST00000619430.2:c.*127del ENSP00000478572.2:n.*127del
ENST00000676670.1:c.*15+112del ENSP00000504807.1:n.*15+112del
ENST00000676741.1:n.2712del
ENST00000677624.1:c.*1050del ENSP00000503979.1:n.*1050del
ENST00000677625.1:c.*127del ENSP00000502857.1:n.*127del
ENST00000677856.1:n.1883del
ENST00000677915.1:c.*527del ENSP00000503118.1:n.*527del
ENST00000678533.1:c.*1072+112del ENSP00000503873.1:n.*1072+112del
ENST00000678592.1:c.*570del ENSP00000504424.1:n.*570del
ENST00000278407.8:c.*127del ENSP00000278407.4:n.*127del
ENST00000340687.10:c.*127del ENSP00000341861.6:n.*127del
ENST00000378323.8:c.*127del ENSP00000367574.4:n.*127del
ENST00000378324.6:c.*127del ENSP00000367575.2:n.*127del
ENST00000403558.1:c.*127del ENSP00000384420.1:n.*127del
ENST00000528996.1:c.831del ENSP00000431226.1:n.831del
ENST00000531797.5:c.*655del ENSP00000432554.1:n.*655del
NM_000062.2:c.*127del , LRG_105t1:c.*127del NP_000053.2:n.*127del
NM_001032295.1:c.*127del NP_001027466.1:n.*127del
NM_000062.3:c.*127del MANE Select NP_000053.2:n.*127del
NM_001032295.2:c.*127del NP_001027466.1:n.*127del