Canonical Allele Identifier: CA1385028960

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877054G= , CM000665.2:g.93877054G=	GRCh38
NC_000003.11:g.93595898G= , CM000665.1:g.93595898G=	GRCh37
NC_000003.10:g.95078588G=	NCBI36
NG_009813.1:g.102037C= , LRG_572:g.102037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1782C=	ENSP00000330021.7:p.Thr594=
ENST00000394236.9:c.1782C= MANE Select	ENSP00000377783.3:p.Thr594=
ENST00000407433.6:c.1737C=	ENSP00000385794.2:p.Thr579=
ENST00000647936.1:c.1644+2109C=	ENSP00000496822.1:n.1644+2109C=
ENST00000648381.1:n.1950C=
ENST00000648853.1:c.1740C=	ENSP00000497262.1:p.Thr580=
ENST00000649103.1:c.1881C=	ENSP00000497962.1:n.1881C=
ENST00000649585.1:c.725C=	ENSP00000498163.1:n.725C=
ENST00000650591.1:c.1878C=	ENSP00000497376.1:p.Thr626=
ENST00000394236.7:c.1782C=	ENSP00000377783.3:p.Thr594=
ENST00000407433.5:c.1389C=	ENSP00000385794.1:p.Thr463=
NM_000313.3:c.1782C= , LRG_572t1:c.1782C=	NP_000304.2:p.Thr594=
NM_001314077.1:c.1878C= , LRG_572t2:c.1878C=	NP_001301006.1:p.Thr626=
NM_000313.4:c.1782C= MANE Select	NP_000304.2:p.Thr594=
NM_001314077.2:c.1878C=	NP_001301006.1:p.Thr626=