Canonical Allele Identifier: CA1385038314

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896622C= , CM000665.2:g.93896622C=	GRCh38
NC_000003.11:g.93615466C= , CM000665.1:g.93615466C=	GRCh37
NC_000003.10:g.95098156C=	NCBI36
NG_009813.1:g.82469G= , LRG_572:g.82469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.919G=	ENSP00000330021.7:p.Ala307=
ENST00000394236.9:c.919G= MANE Select	ENSP00000377783.3:p.Ala307=
ENST00000407433.6:c.874G=	ENSP00000385794.2:p.Ala292=
ENST00000647936.1:c.919G=	ENSP00000496822.1:p.Ala307=
ENST00000648381.1:n.1087G=
ENST00000648853.1:c.877G=	ENSP00000497262.1:p.Ala293=
ENST00000649103.1:c.1018G=	ENSP00000497962.1:n.1018G=
ENST00000650591.1:c.1015G=	ENSP00000497376.1:p.Ala339=
ENST00000394236.7:c.919G=	ENSP00000377783.3:p.Ala307=
ENST00000407433.5:c.526G=	ENSP00000385794.1:p.Ala176=
NM_000313.3:c.919G= , LRG_572t1:c.919G=	NP_000304.2:p.Ala307=
NM_001314077.1:c.1015G= , LRG_572t2:c.1015G=	NP_001301006.1:p.Ala339=
NM_000313.4:c.919G= MANE Select	NP_000304.2:p.Ala307=
NM_001314077.2:c.1015G=	NP_001301006.1:p.Ala339=