Canonical Allele Identifier: CA1385039116

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898478G= , CM000665.2:g.93898478G=	GRCh38
NC_000003.11:g.93617322G= , CM000665.1:g.93617322G=	GRCh37
NC_000003.10:g.95100012G=	NCBI36
NG_009813.1:g.80613C= , LRG_572:g.80613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.819C=	ENSP00000330021.7:p.Phe273=
ENST00000394236.9:c.819C= MANE Select	ENSP00000377783.3:p.Phe273=
ENST00000407433.6:c.774C=	ENSP00000385794.2:p.Phe258=
ENST00000647936.1:c.819C=	ENSP00000496822.1:p.Phe273=
ENST00000648381.1:n.987C=
ENST00000648853.1:c.777C=	ENSP00000497262.1:p.Phe259=
ENST00000649103.1:c.918C=	ENSP00000497962.1:n.918C=
ENST00000650591.1:c.915C=	ENSP00000497376.1:p.Phe305=
ENST00000394236.7:c.819C=	ENSP00000377783.3:p.Phe273=
ENST00000407433.5:c.426C=	ENSP00000385794.1:p.Phe142=
NM_000313.3:c.819C= , LRG_572t1:c.819C=	NP_000304.2:p.Phe273=
NM_001314077.1:c.915C= , LRG_572t2:c.915C=	NP_001301006.1:p.Phe305=
NM_000313.4:c.819C= MANE Select	NP_000304.2:p.Phe273=
NM_001314077.2:c.915C=	NP_001301006.1:p.Phe305=