Canonical Allele Identifier: CA2586972701

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896642dup , CM000665.2:g.93896642dup	GRCh38
NC_000003.11:g.93615486dup , CM000665.1:g.93615486dup	GRCh37
NC_000003.10:g.95098176dup	NCBI36
NG_009813.1:g.82451dup , LRG_572:g.82451dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.901dup	ENSP00000330021.7:p.Tyr301LeufsTer28
ENST00000394236.9:c.901dup MANE Select	ENSP00000377783.3:p.Tyr301LeufsTer28
ENST00000407433.6:c.856dup	ENSP00000385794.2:p.Tyr286LeufsTer28
ENST00000647936.1:c.901dup	ENSP00000496822.1:p.Tyr301LeufsTer28
ENST00000648381.1:n.1069dup
ENST00000648853.1:c.859dup	ENSP00000497262.1:p.Tyr287LeufsTer28
ENST00000649103.1:c.1000dup	ENSP00000497962.1:n.1000dup
ENST00000650591.1:c.997dup	ENSP00000497376.1:p.Tyr333LeufsTer28
ENST00000394236.7:c.901dup	ENSP00000377783.3:p.Tyr301LeufsTer28
ENST00000407433.5:c.508dup	ENSP00000385794.1:p.Tyr170LeufsTer28
NM_000313.3:c.901dup , LRG_572t1:c.901dup	NP_000304.2:p.Tyr301LeufsTer28
NM_001314077.1:c.997dup , LRG_572t2:c.997dup	NP_001301006.1:p.Tyr333LeufsTer28
NM_000313.4:c.901dup MANE Select	NP_000304.2:p.Tyr301LeufsTer28
NM_001314077.2:c.997dup	NP_001301006.1:p.Tyr333LeufsTer28