Canonical Allele Identifier: CA1385026753

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873916_93873917delinsAC , CM000665.2:g.93873916_93873917delinsAC	GRCh38
NC_000003.11:g.93592760_93592761delinsAC , CM000665.1:g.93592760_93592761delinsAC	GRCh37
NC_000003.10:g.95075450_95075451delinsAC	NCBI36
NG_009813.1:g.105174_105175delinsGT , LRG_572:g.105174_105175delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+327_*1+328delinsGT	ENSP00000330021.7:n.*1+327_*1+328delinsGT
ENST00000394236.9:c.*328_*329delinsGT MANE Select	ENSP00000377783.3:n.*328_*329delinsGT
ENST00000407433.6:c.*328_*329delinsGT	ENSP00000385794.2:n.*328_*329delinsGT
ENST00000647936.1:c.*462_*463delinsGT	ENSP00000496822.1:n.*462_*463delinsGT
ENST00000648381.1:n.2527_2528delinsGT
ENST00000648853.1:c.*328_*329delinsGT	ENSP00000497262.1:n.*328_*329delinsGT
ENST00000650591.1:c.*328_*329delinsGT	ENSP00000497376.1:n.*328_*329delinsGT
ENST00000394236.7:c.*328_*329delinsGT	ENSP00000377783.3:n.*328_*329delinsGT
ENST00000407433.5:c.*328_*329delinsGT	ENSP00000385794.1:n.*328_*329delinsGT
NM_000313.3:c.*328_*329delinsGT , LRG_572t1:c.*328_*329delinsGT	NP_000304.2:n.*328_*329delinsGT
NM_001314077.1:c.*328_*329delinsGT , LRG_572t2:c.*328_*329delinsGT	NP_001301006.1:n.*328_*329delinsGT
NM_000313.4:c.*328_*329delinsGT MANE Select	NP_000304.2:n.*328_*329delinsGT
NM_001314077.2:c.*328_*329delinsGT	NP_001301006.1:n.*328_*329delinsGT