Canonical Allele Identifier: CA1385040197

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900847G= , CM000665.2:g.93900847G=	GRCh38
NC_000003.11:g.93619691G= , CM000665.1:g.93619691G=	GRCh37
NC_000003.10:g.95102381G=	NCBI36
NG_009813.1:g.78244C= , LRG_572:g.78244C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.684C=	ENSP00000330021.7:p.Cys228=
ENST00000394236.9:c.684C= MANE Select	ENSP00000377783.3:p.Cys228=
ENST00000407433.6:c.639C=	ENSP00000385794.2:p.Cys213=
ENST00000647936.1:c.684C=	ENSP00000496822.1:p.Cys228=
ENST00000648381.1:n.852C=
ENST00000648853.1:c.642C=	ENSP00000497262.1:p.Cys214=
ENST00000649103.1:c.783C=	ENSP00000497962.1:n.783C=
ENST00000650591.1:c.780C=	ENSP00000497376.1:p.Cys260=
ENST00000394236.7:c.684C=	ENSP00000377783.3:p.Cys228=
ENST00000407433.5:c.291C=	ENSP00000385794.1:p.Cys97=
NM_000313.3:c.684C= , LRG_572t1:c.684C=	NP_000304.2:p.Cys228=
NM_001314077.1:c.780C= , LRG_572t2:c.780C=	NP_001301006.1:p.Cys260=
NM_000313.4:c.684C= MANE Select	NP_000304.2:p.Cys228=
NM_001314077.2:c.780C=	NP_001301006.1:p.Cys260=