Canonical Allele Identifier: CA1385030608

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879211T= , CM000665.2:g.93879211T=	GRCh38
NC_000003.11:g.93598055T= , CM000665.1:g.93598055T=	GRCh37
NC_000003.10:g.95080745T=	NCBI36
NG_009813.1:g.99880A= , LRG_572:g.99880A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1596A=	ENSP00000330021.7:p.Thr532=
ENST00000394236.9:c.1596A= MANE Select	ENSP00000377783.3:p.Thr532=
ENST00000407433.6:c.1551A=	ENSP00000385794.2:p.Thr517=
ENST00000647936.1:c.1596A=	ENSP00000496822.1:p.Thr532=
ENST00000648381.1:n.1764A=
ENST00000648853.1:c.1554A=	ENSP00000497262.1:p.Thr518=
ENST00000649103.1:c.1695A=	ENSP00000497962.1:n.1695A=
ENST00000649585.1:c.539A=	ENSP00000498163.1:n.539A=
ENST00000650591.1:c.1692A=	ENSP00000497376.1:p.Thr564=
ENST00000394236.7:c.1596A=	ENSP00000377783.3:p.Thr532=
ENST00000407433.5:c.1203A=	ENSP00000385794.1:p.Thr401=
NM_000313.3:c.1596A= , LRG_572t1:c.1596A=	NP_000304.2:p.Thr532=
NM_001314077.1:c.1692A= , LRG_572t2:c.1692A=	NP_001301006.1:p.Thr564=
NM_000313.4:c.1596A= MANE Select	NP_000304.2:p.Thr532=
NM_001314077.2:c.1692A=	NP_001301006.1:p.Thr564=