Canonical Allele Identifier: CA1385042579

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905795T= , CM000665.2:g.93905795T=	GRCh38
NC_000003.11:g.93624639T= , CM000665.1:g.93624639T=	GRCh37
NC_000003.10:g.95107329T=	NCBI36
NG_009813.1:g.73296A= , LRG_572:g.73296A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.590A=	ENSP00000330021.7:p.Lys197=
ENST00000394236.9:c.590A= MANE Select	ENSP00000377783.3:p.Lys197=
ENST00000407433.6:c.556+34A=	ENSP00000385794.2:n.556+34A=
ENST00000647936.1:c.590A=	ENSP00000496822.1:p.Lys197=
ENST00000648381.1:n.758A=
ENST00000648853.1:c.548A=	ENSP00000497262.1:p.Lys183=
ENST00000649103.1:c.689A=	ENSP00000497962.1:n.689A=
ENST00000650591.1:c.686A=	ENSP00000497376.1:p.Lys229=
ENST00000348974.4:c.686A=	ENSP00000330021.6:p.Lys229=
ENST00000394236.7:c.590A=	ENSP00000377783.3:p.Lys197=
ENST00000407433.5:c.197A=	ENSP00000385794.1:p.Lys66=
NM_000313.3:c.590A= , LRG_572t1:c.590A=	NP_000304.2:p.Lys197=
NM_001314077.1:c.686A= , LRG_572t2:c.686A=	NP_001301006.1:p.Lys229=
NM_000313.4:c.590A= MANE Select	NP_000304.2:p.Lys197=
NM_001314077.2:c.686A=	NP_001301006.1:p.Lys229=