Canonical Allele Identifier: CA1385028941

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877044C= , CM000665.2:g.93877044C=	GRCh38
NC_000003.11:g.93595888C= , CM000665.1:g.93595888C=	GRCh37
NC_000003.10:g.95078578C=	NCBI36
NG_009813.1:g.102047G= , LRG_572:g.102047G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1792G=	ENSP00000330021.7:p.Glu598=
ENST00000394236.9:c.1792G= MANE Select	ENSP00000377783.3:p.Glu598=
ENST00000407433.6:c.1747G=	ENSP00000385794.2:p.Glu583=
ENST00000647936.1:c.1644+2119G=	ENSP00000496822.1:n.1644+2119G=
ENST00000648381.1:n.1960G=
ENST00000648853.1:c.1750G=	ENSP00000497262.1:p.Glu584=
ENST00000649585.1:c.735G=	ENSP00000498163.1:n.735G=
ENST00000650591.1:c.1888G=	ENSP00000497376.1:p.Glu630=
ENST00000394236.7:c.1792G=	ENSP00000377783.3:p.Glu598=
ENST00000407433.5:c.1399G=	ENSP00000385794.1:p.Glu467=
NM_000313.3:c.1792G= , LRG_572t1:c.1792G=	NP_000304.2:p.Glu598=
NM_001314077.1:c.1888G= , LRG_572t2:c.1888G=	NP_001301006.1:p.Glu630=
NM_000313.4:c.1792G= MANE Select	NP_000304.2:p.Glu598=
NM_001314077.2:c.1888G=	NP_001301006.1:p.Glu630=