Canonical Allele Identifier: CA1385030632

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879264G= , CM000665.2:g.93879264G=	GRCh38
NC_000003.11:g.93598108G= , CM000665.1:g.93598108G=	GRCh37
NC_000003.10:g.95080798G=	NCBI36
NG_009813.1:g.99827C= , LRG_572:g.99827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1543C=	ENSP00000330021.7:p.Arg515=
ENST00000394236.9:c.1543C= MANE Select	ENSP00000377783.3:p.Arg515=
ENST00000407433.6:c.1498C=	ENSP00000385794.2:p.Arg500=
ENST00000647936.1:c.1543C=	ENSP00000496822.1:p.Arg515=
ENST00000648381.1:n.1711C=
ENST00000648853.1:c.1501C=	ENSP00000497262.1:p.Arg501=
ENST00000649103.1:c.1642C=	ENSP00000497962.1:n.1642C=
ENST00000649585.1:c.486C=	ENSP00000498163.1:n.486C=
ENST00000650591.1:c.1639C=	ENSP00000497376.1:p.Arg547=
ENST00000394236.7:c.1543C=	ENSP00000377783.3:p.Arg515=
ENST00000407433.5:c.1150C=	ENSP00000385794.1:p.Arg384=
NM_000313.3:c.1543C= , LRG_572t1:c.1543C=	NP_000304.2:p.Arg515=
NM_001314077.1:c.1639C= , LRG_572t2:c.1639C=	NP_001301006.1:p.Arg547=
NM_000313.4:c.1543C= MANE Select	NP_000304.2:p.Arg515=
NM_001314077.2:c.1639C=	NP_001301006.1:p.Arg547=