Canonical Allele Identifier: CA1385030635

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879274G= , CM000665.2:g.93879274G=	GRCh38
NC_000003.11:g.93598118G= , CM000665.1:g.93598118G=	GRCh37
NC_000003.10:g.95080808G=	NCBI36
NG_009813.1:g.99817C= , LRG_572:g.99817C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1533C=	ENSP00000330021.7:p.Thr511=
ENST00000394236.9:c.1533C= MANE Select	ENSP00000377783.3:p.Thr511=
ENST00000407433.6:c.1488C=	ENSP00000385794.2:p.Thr496=
ENST00000647936.1:c.1533C=	ENSP00000496822.1:p.Thr511=
ENST00000648381.1:n.1701C=
ENST00000648853.1:c.1491C=	ENSP00000497262.1:p.Thr497=
ENST00000649103.1:c.1632C=	ENSP00000497962.1:n.1632C=
ENST00000649585.1:c.476C=	ENSP00000498163.1:n.476C=
ENST00000650591.1:c.1629C=	ENSP00000497376.1:p.Thr543=
ENST00000394236.7:c.1533C=	ENSP00000377783.3:p.Thr511=
ENST00000407433.5:c.1140C=	ENSP00000385794.1:p.Thr380=
NM_000313.3:c.1533C= , LRG_572t1:c.1533C=	NP_000304.2:p.Thr511=
NM_001314077.1:c.1629C= , LRG_572t2:c.1629C=	NP_001301006.1:p.Thr543=
NM_000313.4:c.1533C= MANE Select	NP_000304.2:p.Thr511=
NM_001314077.2:c.1629C=	NP_001301006.1:p.Thr543=