Canonical Allele Identifier: CA2695214276
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614502dup , CM000673.2:g.57614502dup GRCh38
NC_000011.9:g.57381975dup , CM000673.1:g.57381975dup GRCh37
NC_000011.8:g.57138551dup NCBI36
NG_009625.1:g.21949dup , LRG_105:g.21949dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1424dup MANE Select ENSP00000278407.4:p.Pro476AlafsTer22
ENST00000528996.2:c.*321dup ENSP00000431226.2:n.*321dup
ENST00000531605.2:c.*1200dup ENSP00000503752.1:n.*1200dup
ENST00000619430.2:c.1220dup ENSP00000478572.2:p.Pro408AlafsTer22
ENST00000676670.1:c.1424dup ENSP00000504807.1:p.Pro476AlafsTer22
ENST00000676741.1:n.2506dup
ENST00000677624.1:c.*844dup ENSP00000503979.1:n.*844dup
ENST00000677625.1:c.1370dup ENSP00000502857.1:p.Pro458AlafsTer22
ENST00000677856.1:n.1677dup
ENST00000677915.1:c.*321dup ENSP00000503118.1:n.*321dup
ENST00000678533.1:c.*978dup ENSP00000503873.1:n.*978dup
ENST00000678592.1:c.*364dup ENSP00000504424.1:n.*364dup
ENST00000278407.8:c.1424dup ENSP00000278407.4:p.Pro476AlafsTer22
ENST00000340687.10:c.1313dup ENSP00000341861.6:p.Pro439AlafsTer22
ENST00000378323.8:c.1439dup ENSP00000367574.4:p.Pro481AlafsTer22
ENST00000378324.6:c.1268dup ENSP00000367575.2:p.Pro424AlafsTer22
ENST00000403558.1:c.1553dup ENSP00000384420.1:p.Pro519AlafsTer22
ENST00000528996.1:c.625dup ENSP00000431226.1:n.625dup
ENST00000530113.1:n.881dup
ENST00000531133.5:c.925dup ENSP00000435431.1:n.925dup
ENST00000531797.5:c.*449dup ENSP00000432554.1:n.*449dup
ENST00000619430.1:c.555dup ENSP00000478572.1:n.555dup
NM_000062.2:c.1424dup , LRG_105t1:c.1424dup NP_000053.2:p.Pro476AlafsTer22
NM_001032295.1:c.1424dup NP_001027466.1:p.Pro476AlafsTer22
NM_000062.3:c.1424dup MANE Select NP_000053.2:p.Pro476AlafsTer22
NM_001032295.2:c.1424dup NP_001027466.1:p.Pro476AlafsTer22