Canonical Allele Identifier: CA1385038298

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896594C= , CM000665.2:g.93896594C=	GRCh38
NC_000003.11:g.93615438C= , CM000665.1:g.93615438C=	GRCh37
NC_000003.10:g.95098128C=	NCBI36
NG_009813.1:g.82497G= , LRG_572:g.82497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.947G=	ENSP00000330021.7:p.Arg316=
ENST00000394236.9:c.947G= MANE Select	ENSP00000377783.3:p.Arg316=
ENST00000407433.6:c.902G=	ENSP00000385794.2:p.Arg301=
ENST00000647936.1:c.947G=	ENSP00000496822.1:p.Arg316=
ENST00000648381.1:n.1115G=
ENST00000648853.1:c.905G=	ENSP00000497262.1:p.Arg302=
ENST00000649103.1:c.1046G=	ENSP00000497962.1:n.1046G=
ENST00000650591.1:c.1043G=	ENSP00000497376.1:p.Arg348=
ENST00000394236.7:c.947G=	ENSP00000377783.3:p.Arg316=
ENST00000407433.5:c.554G=	ENSP00000385794.1:p.Arg185=
NM_000313.3:c.947G= , LRG_572t1:c.947G=	NP_000304.2:p.Arg316=
NM_001314077.1:c.1043G= , LRG_572t2:c.1043G=	NP_001301006.1:p.Arg348=
NM_000313.4:c.947G= MANE Select	NP_000304.2:p.Arg316=
NM_001314077.2:c.1043G=	NP_001301006.1:p.Arg348=