Canonical Allele Identifier: CA1385042581

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905799T= , CM000665.2:g.93905799T=	GRCh38
NC_000003.11:g.93624643T= , CM000665.1:g.93624643T=	GRCh37
NC_000003.10:g.95107333T=	NCBI36
NG_009813.1:g.73292A= , LRG_572:g.73292A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.586A= MANE Select	NP_000304.2:p.Lys196=
ENST00000394236.9:c.586A= MANE Select	ENSP00000377783.3:p.Lys196=
NM_000313.3:c.586A= , LRG_572t1:c.586A=	NP_000304.2:p.Lys196=
NM_001314077.1:c.682A= , LRG_572t2:c.682A=	NP_001301006.1:p.Lys228=
NM_001314077.2:c.682A=	NP_001301006.1:p.Lys228=
ENST00000348974.4:c.682A=	ENSP00000330021.6:p.Lys228=
ENST00000348974.5:c.586A=	ENSP00000330021.7:p.Lys196=
ENST00000394236.7:c.586A=	ENSP00000377783.3:p.Lys196=
ENST00000407433.5:c.193A=	ENSP00000385794.1:p.Lys65=
ENST00000407433.6:c.556+30A=	ENSP00000385794.2:n.556+30A=
ENST00000647936.1:c.586A=	ENSP00000496822.1:p.Lys196=
ENST00000648381.1:n.754A=
ENST00000648853.1:c.544A=	ENSP00000497262.1:p.Lys182=
ENST00000649103.1:c.685A=	ENSP00000497962.1:n.685A=
ENST00000650591.1:c.682A=	ENSP00000497376.1:p.Lys228=