Canonical Allele Identifier: CA1385028997

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877076G= , CM000665.2:g.93877076G=	GRCh38
NC_000003.11:g.93595920G= , CM000665.1:g.93595920G=	GRCh37
NC_000003.10:g.95078610G=	NCBI36
NG_009813.1:g.102015C= , LRG_572:g.102015C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1760C=	ENSP00000330021.7:p.Ser587=
ENST00000394236.9:c.1760C= MANE Select	ENSP00000377783.3:p.Ser587=
ENST00000407433.6:c.1715C=	ENSP00000385794.2:p.Ser572=
ENST00000647936.1:c.1644+2087C=	ENSP00000496822.1:n.1644+2087C=
ENST00000648381.1:n.1928C=
ENST00000648853.1:c.1718C=	ENSP00000497262.1:p.Ser573=
ENST00000649103.1:c.1859C=	ENSP00000497962.1:n.1859C=
ENST00000649585.1:c.703C=	ENSP00000498163.1:n.703C=
ENST00000650591.1:c.1856C=	ENSP00000497376.1:p.Ser619=
ENST00000394236.7:c.1760C=	ENSP00000377783.3:p.Ser587=
ENST00000407433.5:c.1367C=	ENSP00000385794.1:p.Ser456=
NM_000313.3:c.1760C= , LRG_572t1:c.1760C=	NP_000304.2:p.Ser587=
NM_001314077.1:c.1856C= , LRG_572t2:c.1856C=	NP_001301006.1:p.Ser619=
NM_000313.4:c.1760C= MANE Select	NP_000304.2:p.Ser587=
NM_001314077.2:c.1856C=	NP_001301006.1:p.Ser619=