Canonical Allele Identifier: CA1385038326

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896649C= , CM000665.2:g.93896649C=	GRCh38
NC_000003.11:g.93615493C= , CM000665.1:g.93615493C=	GRCh37
NC_000003.10:g.95098183C=	NCBI36
NG_009813.1:g.82442G= , LRG_572:g.82442G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.892G=	ENSP00000330021.7:p.Glu298=
ENST00000394236.9:c.892G= MANE Select	ENSP00000377783.3:p.Glu298=
ENST00000407433.6:c.847G=	ENSP00000385794.2:p.Glu283=
ENST00000647936.1:c.892G=	ENSP00000496822.1:p.Glu298=
ENST00000648381.1:n.1060G=
ENST00000648853.1:c.850G=	ENSP00000497262.1:p.Glu284=
ENST00000649103.1:c.991G=	ENSP00000497962.1:n.991G=
ENST00000650591.1:c.988G=	ENSP00000497376.1:p.Glu330=
ENST00000394236.7:c.892G=	ENSP00000377783.3:p.Glu298=
ENST00000407433.5:c.499G=	ENSP00000385794.1:p.Glu167=
NM_000313.3:c.892G= , LRG_572t1:c.892G=	NP_000304.2:p.Glu298=
NM_001314077.1:c.988G= , LRG_572t2:c.988G=	NP_001301006.1:p.Glu330=
NM_000313.4:c.892G= MANE Select	NP_000304.2:p.Glu298=
NM_001314077.2:c.988G=	NP_001301006.1:p.Glu330=