Canonical Allele Identifier: CA1385033079

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93884827C= , CM000665.2:g.93884827C=	GRCh38
NC_000003.11:g.93603671C= , CM000665.1:g.93603671C=	GRCh37
NC_000003.10:g.95086361C=	NCBI36
NG_009813.1:g.94264G= , LRG_572:g.94264G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.1393G= MANE Select	NP_000304.2:p.Glu465=
ENST00000394236.9:c.1393G= MANE Select	ENSP00000377783.3:p.Glu465=
NM_000313.3:c.1393G= , LRG_572t1:c.1393G=	NP_000304.2:p.Glu465=
NM_001314077.1:c.1489G= , LRG_572t2:c.1489G=	NP_001301006.1:p.Glu497=
NM_001314077.2:c.1489G=	NP_001301006.1:p.Glu497=
ENST00000348974.5:c.1393G=	ENSP00000330021.7:p.Glu465=
ENST00000394236.7:c.1393G=	ENSP00000377783.3:p.Glu465=
ENST00000407433.5:c.1000G=	ENSP00000385794.1:p.Glu334=
ENST00000407433.6:c.1348G=	ENSP00000385794.2:p.Glu450=
ENST00000647936.1:c.1393G=	ENSP00000496822.1:p.Glu465=
ENST00000648381.1:n.1561G=
ENST00000648853.1:c.1351G=	ENSP00000497262.1:p.Glu451=
ENST00000649103.1:c.1492G=	ENSP00000497962.1:n.1492G=
ENST00000649585.1:c.148G=	ENSP00000498163.1:p.Glu50=
ENST00000650591.1:c.1489G=	ENSP00000497376.1:p.Glu497=