Canonical Allele Identifier: CA1385039137

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898552C= , CM000665.2:g.93898552C=	GRCh38
NC_000003.11:g.93617396C= , CM000665.1:g.93617396C=	GRCh37
NC_000003.10:g.95100086C=	NCBI36
NG_009813.1:g.80539G= , LRG_572:g.80539G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.745G=	ENSP00000330021.7:p.Glu249=
ENST00000394236.9:c.745G= MANE Select	ENSP00000377783.3:p.Glu249=
ENST00000407433.6:c.700G=	ENSP00000385794.2:p.Glu234=
ENST00000647936.1:c.745G=	ENSP00000496822.1:p.Glu249=
ENST00000648381.1:n.913G=
ENST00000648853.1:c.703G=	ENSP00000497262.1:p.Glu235=
ENST00000649103.1:c.844G=	ENSP00000497962.1:n.844G=
ENST00000650591.1:c.841G=	ENSP00000497376.1:p.Glu281=
ENST00000394236.7:c.745G=	ENSP00000377783.3:p.Glu249=
ENST00000407433.5:c.352G=	ENSP00000385794.1:p.Glu118=
NM_000313.3:c.745G= , LRG_572t1:c.745G=	NP_000304.2:p.Glu249=
NM_001314077.1:c.841G= , LRG_572t2:c.841G=	NP_001301006.1:p.Glu281=
NM_000313.4:c.745G= MANE Select	NP_000304.2:p.Glu249=
NM_001314077.2:c.841G=	NP_001301006.1:p.Glu281=