Canonical Allele Identifier: CA2695214118
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606179_57606180del , CM000673.2:g.57606179_57606180del GRCh38
NC_000011.9:g.57373652_57373653del , CM000673.1:g.57373652_57373653del GRCh37
NC_000011.8:g.57130228_57130229del NCBI36
NG_009625.1:g.13626_13627del , LRG_105:g.13626_13627del

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.855_856del MANE Select ENSP00000278407.4:p.Arg286ProfsTer18
ENST00000528996.2:c.59-5547_59-5546del ENSP00000431226.2:n.59-5547_59-5546del
ENST00000531605.2:c.*631_*632del ENSP00000503752.1:n.*631_*632del
ENST00000619430.2:c.686-229_686-228del ENSP00000478572.2:n.686-229_686-228del
ENST00000676670.1:c.855_856del ENSP00000504807.1:p.Arg286ProfsTer18
ENST00000676741.1:n.1937_1938del
ENST00000677624.1:c.*275_*276del ENSP00000503979.1:n.*275_*276del
ENST00000677625.1:c.855_856del ENSP00000502857.1:p.Arg286ProfsTer18
ENST00000677856.1:n.914_915del
ENST00000677915.1:c.685+4010_685+4011del ENSP00000503118.1:n.685+4010_685+4011del
ENST00000678533.1:c.*409_*410del ENSP00000503873.1:n.*409_*410del
ENST00000678592.1:c.855_856del ENSP00000504424.1:p.Arg286ProfsTer18
ENST00000278407.8:c.855_856del ENSP00000278407.4:p.Arg286ProfsTer18
ENST00000340687.10:c.855_856del ENSP00000341861.6:p.Arg286ProfsTer18
ENST00000378323.8:c.870_871del ENSP00000367574.4:p.Arg291ProfsTer18
ENST00000378324.6:c.699_700del ENSP00000367575.2:p.Arg234ProfsTer18
ENST00000403558.1:c.957_958del ENSP00000384420.1:p.Arg320ProfsTer11
ENST00000531133.5:c.356_357del ENSP00000435431.1:n.356_357del
ENST00000531797.5:c.*54+4010_*54+4011del ENSP00000432554.1:n.*54+4010_*54+4011del
ENST00000619430.1:c.349-5726_349-5725del ENSP00000478572.1:n.349-5726_349-5725del
NM_000062.2:c.855_856del , LRG_105t1:c.855_856del NP_000053.2:p.Arg286ProfsTer18
NM_001032295.1:c.855_856del NP_001027466.1:p.Arg286ProfsTer18
NM_000062.3:c.855_856del MANE Select NP_000053.2:p.Arg286ProfsTer18
NM_001032295.2:c.855_856del NP_001027466.1:p.Arg286ProfsTer18