Canonical Allele Identifier: CA2757500347

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873760_93873761dup , CM000665.2:g.93873760_93873761dup	GRCh38
NC_000003.11:g.93592604_93592605dup , CM000665.1:g.93592604_93592605dup	GRCh37
NC_000003.10:g.95075294_95075295dup	NCBI36
NG_009813.1:g.105330_105331dup , LRG_572:g.105330_105331dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-348_*2-347dup	ENSP00000330021.7:n.*2-348_*2-347dup
ENST00000394236.9:c.*484_*485dup MANE Select	ENSP00000377783.3:n.*484_*485dup
ENST00000407433.6:c.*484_*485dup	ENSP00000385794.2:n.*484_*485dup
ENST00000647936.1:c.*618_*619dup	ENSP00000496822.1:n.*618_*619dup
ENST00000648381.1:n.2683_2684dup
ENST00000648853.1:c.*484_*485dup	ENSP00000497262.1:n.*484_*485dup
ENST00000650591.1:c.*484_*485dup	ENSP00000497376.1:n.*484_*485dup
ENST00000394236.7:c.*484_*485dup	ENSP00000377783.3:n.*484_*485dup
ENST00000407433.5:c.*484_*485dup	ENSP00000385794.1:n.*484_*485dup
NM_000313.3:c.*484_*485dup , LRG_572t1:c.*484_*485dup	NP_000304.2:n.*484_*485dup
NM_001314077.1:c.*484_*485dup , LRG_572t2:c.*484_*485dup	NP_001301006.1:n.*484_*485dup
NM_000313.4:c.*484_*485dup MANE Select	NP_000304.2:n.*484_*485dup
NM_001314077.2:c.*484_*485dup	NP_001301006.1:n.*484_*485dup