Canonical Allele Identifier: CA1385030595

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879173T= , CM000665.2:g.93879173T=	GRCh38
NC_000003.11:g.93598017T= , CM000665.1:g.93598017T=	GRCh37
NC_000003.10:g.95080707T=	NCBI36
NG_009813.1:g.99918A= , LRG_572:g.99918A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1634A=	ENSP00000330021.7:p.Glu545=
ENST00000394236.9:c.1634A= MANE Select	ENSP00000377783.3:p.Glu545=
ENST00000407433.6:c.1589A=	ENSP00000385794.2:p.Glu530=
ENST00000647936.1:c.1634A=	ENSP00000496822.1:p.Glu545=
ENST00000648381.1:n.1802A=
ENST00000648853.1:c.1592A=	ENSP00000497262.1:p.Glu531=
ENST00000649103.1:c.1733A=	ENSP00000497962.1:n.1733A=
ENST00000649585.1:c.577A=	ENSP00000498163.1:n.577A=
ENST00000650591.1:c.1730A=	ENSP00000497376.1:p.Glu577=
ENST00000394236.7:c.1634A=	ENSP00000377783.3:p.Glu545=
ENST00000407433.5:c.1241A=	ENSP00000385794.1:p.Glu414=
NM_000313.3:c.1634A= , LRG_572t1:c.1634A=	NP_000304.2:p.Glu545=
NM_001314077.1:c.1730A= , LRG_572t2:c.1730A=	NP_001301006.1:p.Glu577=
NM_000313.4:c.1634A= MANE Select	NP_000304.2:p.Glu545=
NM_001314077.2:c.1730A=	NP_001301006.1:p.Glu577=