Canonical Allele Identifier: CA2573147264
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611873del , CM000673.2:g.57611873del GRCh38
NC_000011.9:g.57379346del , CM000673.1:g.57379346del GRCh37
NC_000011.8:g.57135922del NCBI36
NG_009625.1:g.19320del , LRG_105:g.19320del

Transcript Alleles

HGVS Amino-acid Change
NM_000062.3:c.1186del MANE Select NP_000053.2:p.Leu396Ter
ENST00000278407.9:c.1186del MANE Select ENSP00000278407.4:p.Leu396Ter
NM_000062.2:c.1186del , LRG_105t1:c.1186del NP_000053.2:p.Leu396Ter
NM_001032295.1:c.1186del NP_001027466.1:p.Leu396Ter
NM_001032295.2:c.1186del NP_001027466.1:p.Leu396Ter
ENST00000278407.8:c.1186del ENSP00000278407.4:p.Leu396Ter
ENST00000340687.10:c.1075del ENSP00000341861.6:p.Leu359Ter
ENST00000378323.8:c.1201del ENSP00000367574.4:p.Leu401Ter
ENST00000378324.6:c.1030del ENSP00000367575.2:p.Leu344Ter
ENST00000403558.1:c.1315del ENSP00000384420.1:p.Leu439Ter
ENST00000528996.1:c.387del ENSP00000431226.1:n.387del
ENST00000528996.2:c.*83del ENSP00000431226.2:n.*83del
ENST00000530113.1:n.643del
ENST00000531133.5:c.687del ENSP00000435431.1:n.687del
ENST00000531605.2:c.*962del ENSP00000503752.1:n.*962del
ENST00000531797.5:c.*211del ENSP00000432554.1:n.*211del
ENST00000619430.1:c.349-32del ENSP00000478572.1:n.349-32del
ENST00000619430.2:c.982del ENSP00000478572.2:p.Leu328Ter
ENST00000676670.1:c.1186del ENSP00000504807.1:p.Leu396Ter
ENST00000676741.1:n.2268del
ENST00000677624.1:c.*606del ENSP00000503979.1:n.*606del
ENST00000677625.1:c.1132del ENSP00000502857.1:p.Leu378Ter
ENST00000677856.1:n.1439del
ENST00000677915.1:c.*83del ENSP00000503118.1:n.*83del
ENST00000678533.1:c.*740del ENSP00000503873.1:n.*740del
ENST00000678592.1:c.*126del ENSP00000504424.1:n.*126del