Canonical Allele Identifier: CA1385038328

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896655T= , CM000665.2:g.93896655T=	GRCh38
NC_000003.11:g.93615499T= , CM000665.1:g.93615499T=	GRCh37
NC_000003.10:g.95098189T=	NCBI36
NG_009813.1:g.82436A= , LRG_572:g.82436A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.886A=	ENSP00000330021.7:p.Lys296=
ENST00000394236.9:c.886A= MANE Select	ENSP00000377783.3:p.Lys296=
ENST00000407433.6:c.841A=	ENSP00000385794.2:p.Lys281=
ENST00000647936.1:c.886A=	ENSP00000496822.1:p.Lys296=
ENST00000648381.1:n.1054A=
ENST00000648853.1:c.844A=	ENSP00000497262.1:p.Lys282=
ENST00000649103.1:c.985A=	ENSP00000497962.1:n.985A=
ENST00000650591.1:c.982A=	ENSP00000497376.1:p.Lys328=
ENST00000394236.7:c.886A=	ENSP00000377783.3:p.Lys296=
ENST00000407433.5:c.493A=	ENSP00000385794.1:p.Lys165=
NM_000313.3:c.886A= , LRG_572t1:c.886A=	NP_000304.2:p.Lys296=
NM_001314077.1:c.982A= , LRG_572t2:c.982A=	NP_001301006.1:p.Lys328=
NM_000313.4:c.886A= MANE Select	NP_000304.2:p.Lys296=
NM_001314077.2:c.982A=	NP_001301006.1:p.Lys328=