Canonical Allele Identifier: CA2838032248

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611933_57611934insGCTCTCAAATCA , CM000673.2:g.57611933_57611934insGCTCTCAAATCA	GRCh38
NC_000011.9:g.57379406_57379407insGCTCTCAAATCA , CM000673.1:g.57379406_57379407insGCTCTCAAATCA	GRCh37
NC_000011.8:g.57135982_57135983insGCTCTCAAATCA	NCBI36
NG_009625.1:g.19380_19381insGCTCTCAAATCA , LRG_105:g.19380_19381insGCTCTCAAATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1246_1247insGCTCTCAAATCA MANE Select	ENSP00000278407.4:p.Leu416delinsCysSerGlnIleMet
ENST00000528996.2:c.*143_*144insGCTCTCAAATCA	ENSP00000431226.2:n.*143_*144insGCTCTCAAATCA
ENST00000531605.2:c.*1022_*1023insGCTCTCAAATCA	ENSP00000503752.1:n.*1022_*1023insGCTCTCAAATCA
ENST00000619430.2:c.1042_1043insGCTCTCAAATCA	ENSP00000478572.2:p.Leu348delinsCysSerGlnIleMet
ENST00000676670.1:c.1246_1247insGCTCTCAAATCA	ENSP00000504807.1:p.Leu416delinsCysSerGlnIleMet
ENST00000676741.1:n.2328_2329insGCTCTCAAATCA
ENST00000677624.1:c.*666_*667insGCTCTCAAATCA	ENSP00000503979.1:n.*666_*667insGCTCTCAAATCA
ENST00000677625.1:c.1192_1193insGCTCTCAAATCA	ENSP00000502857.1:p.Leu398delinsCysSerGlnIleMet
ENST00000677856.1:n.1499_1500insGCTCTCAAATCA
ENST00000677915.1:c.*143_*144insGCTCTCAAATCA	ENSP00000503118.1:n.*143_*144insGCTCTCAAATCA
ENST00000678533.1:c.*800_*801insGCTCTCAAATCA	ENSP00000503873.1:n.*800_*801insGCTCTCAAATCA
ENST00000678592.1:c.*186_*187insGCTCTCAAATCA	ENSP00000504424.1:n.*186_*187insGCTCTCAAATCA
ENST00000278407.8:c.1246_1247insGCTCTCAAATCA	ENSP00000278407.4:p.Leu416delinsCysSerGlnIleMet
ENST00000340687.10:c.1135_1136insGCTCTCAAATCA	ENSP00000341861.6:p.Leu379delinsCysSerGlnIleMet
ENST00000378323.8:c.1261_1262insGCTCTCAAATCA	ENSP00000367574.4:p.Leu421delinsCysSerGlnIleMet
ENST00000378324.6:c.1090_1091insGCTCTCAAATCA	ENSP00000367575.2:p.Leu364delinsCysSerGlnIleMet
ENST00000403558.1:c.1375_1376insGCTCTCAAATCA	ENSP00000384420.1:p.Leu459delinsCysSerGlnIleMet
ENST00000528996.1:c.447_448insGCTCTCAAATCA	ENSP00000431226.1:n.447_448insGCTCTCAAATCA
ENST00000530113.1:n.703_704insGCTCTCAAATCA
ENST00000531133.5:c.747_748insGCTCTCAAATCA	ENSP00000435431.1:n.747_748insGCTCTCAAATCA
ENST00000531797.5:c.*271_*272insGCTCTCAAATCA	ENSP00000432554.1:n.*271_*272insGCTCTCAAATCA
ENST00000619430.1:c.377_378insGCTCTCAAATCA	ENSP00000478572.1:p.Ile126delinsMetLeuSerAsnHis
NM_000062.2:c.1246_1247insGCTCTCAAATCA , LRG_105t1:c.1246_1247insGCTCTCAAATCA	NP_000053.2:p.Leu416delinsCysSerGlnIleMet
NM_001032295.1:c.1246_1247insGCTCTCAAATCA	NP_001027466.1:p.Leu416delinsCysSerGlnIleMet
NM_000062.3:c.1246_1247insGCTCTCAAATCA MANE Select	NP_000053.2:p.Leu416delinsCysSerGlnIleMet
NM_001032295.2:c.1246_1247insGCTCTCAAATCA	NP_001027466.1:p.Leu416delinsCysSerGlnIleMet