Canonical Allele Identifier: CA1385039143

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898566A= , CM000665.2:g.93898566A=	GRCh38
NC_000003.11:g.93617410A= , CM000665.1:g.93617410A=	GRCh37
NC_000003.10:g.95100100A=	NCBI36
NG_009813.1:g.80525T= , LRG_572:g.80525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.731T=	ENSP00000330021.7:p.Ile244=
ENST00000394236.9:c.731T= MANE Select	ENSP00000377783.3:p.Ile244=
ENST00000407433.6:c.686T=	ENSP00000385794.2:p.Ile229=
ENST00000647936.1:c.731T=	ENSP00000496822.1:p.Ile244=
ENST00000648381.1:n.899T=
ENST00000648853.1:c.689T=	ENSP00000497262.1:p.Ile230=
ENST00000649103.1:c.830T=	ENSP00000497962.1:n.830T=
ENST00000650591.1:c.827T=	ENSP00000497376.1:p.Ile276=
ENST00000394236.7:c.731T=	ENSP00000377783.3:p.Ile244=
ENST00000407433.5:c.338T=	ENSP00000385794.1:p.Ile113=
NM_000313.3:c.731T= , LRG_572t1:c.731T=	NP_000304.2:p.Ile244=
NM_001314077.1:c.827T= , LRG_572t2:c.827T=	NP_001301006.1:p.Ile276=
NM_000313.4:c.731T= MANE Select	NP_000304.2:p.Ile244=
NM_001314077.2:c.827T=	NP_001301006.1:p.Ile276=