Canonical Allele Identifier: CA1975538985
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614305_57614306delinsGT , CM000673.2:g.57614305_57614306delinsGT GRCh38
NC_000011.9:g.57381778_57381779delinsGT , CM000673.1:g.57381778_57381779delinsGT GRCh37
NC_000011.8:g.57138354_57138355delinsGT NCBI36
NG_009625.1:g.21752_21753delinsGT , LRG_105:g.21752_21753delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1250-23_1250-22delinsGT MANE Select ENSP00000278407.4:n.1250-23_1250-22delinsGT
ENST00000528996.2:c.*147-23_*147-22delinsGT ENSP00000431226.2:n.*147-23_*147-22delinsGT
ENST00000531605.2:c.*1026-23_*1026-22delinsGT ENSP00000503752.1:n.*1026-23_*1026-22delinsGT
ENST00000619430.2:c.1046-23_1046-22delinsGT ENSP00000478572.2:n.1046-23_1046-22delinsGT
ENST00000676670.1:c.1250-23_1250-22delinsGT ENSP00000504807.1:n.1250-23_1250-22delinsGT
ENST00000676741.1:n.2332-23_2332-22delinsGT
ENST00000677624.1:c.*670-23_*670-22delinsGT ENSP00000503979.1:n.*670-23_*670-22delinsGT
ENST00000677625.1:c.1196-23_1196-22delinsGT ENSP00000502857.1:n.1196-23_1196-22delinsGT
ENST00000677856.1:n.1503-23_1503-22delinsGT
ENST00000677915.1:c.*147-23_*147-22delinsGT ENSP00000503118.1:n.*147-23_*147-22delinsGT
ENST00000678533.1:c.*804-23_*804-22delinsGT ENSP00000503873.1:n.*804-23_*804-22delinsGT
ENST00000678592.1:c.*190-23_*190-22delinsGT ENSP00000504424.1:n.*190-23_*190-22delinsGT
ENST00000278407.8:c.1250-23_1250-22delinsGT ENSP00000278407.4:n.1250-23_1250-22delinsGT
ENST00000340687.10:c.1139-23_1139-22delinsGT ENSP00000341861.6:n.1139-23_1139-22delinsGT
ENST00000378323.8:c.1265-23_1265-22delinsGT ENSP00000367574.4:n.1265-23_1265-22delinsGT
ENST00000378324.6:c.1094-23_1094-22delinsGT ENSP00000367575.2:n.1094-23_1094-22delinsGT
ENST00000403558.1:c.1379-23_1379-22delinsGT ENSP00000384420.1:n.1379-23_1379-22delinsGT
ENST00000528996.1:c.451-23_451-22delinsGT ENSP00000431226.1:n.451-23_451-22delinsGT
ENST00000530113.1:n.707-23_707-22delinsGT
ENST00000531133.5:c.751-23_751-22delinsGT ENSP00000435431.1:n.751-23_751-22delinsGT
ENST00000531797.5:c.*275-23_*275-22delinsGT ENSP00000432554.1:n.*275-23_*275-22delinsGT
ENST00000619430.1:c.381-23_381-22delinsGT ENSP00000478572.1:n.381-23_381-22delinsGT
NM_000062.2:c.1250-23_1250-22delinsGT , LRG_105t1:c.1250-23_1250-22delinsGT NP_000053.2:n.1250-23_1250-22delinsGT
NM_001032295.1:c.1250-23_1250-22delinsGT NP_001027466.1:n.1250-23_1250-22delinsGT
NM_000062.3:c.1250-23_1250-22delinsGT MANE Select NP_000053.2:n.1250-23_1250-22delinsGT
NM_001032295.2:c.1250-23_1250-22delinsGT NP_001027466.1:n.1250-23_1250-22delinsGT