Canonical Allele Identifier: CA1385038313

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896621G= , CM000665.2:g.93896621G=	GRCh38
NC_000003.11:g.93615465G= , CM000665.1:g.93615465G=	GRCh37
NC_000003.10:g.95098155G=	NCBI36
NG_009813.1:g.82470C= , LRG_572:g.82470C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.920C=	ENSP00000330021.7:p.Ala307=
ENST00000394236.9:c.920C= MANE Select	ENSP00000377783.3:p.Ala307=
ENST00000407433.6:c.875C=	ENSP00000385794.2:p.Ala292=
ENST00000647936.1:c.920C=	ENSP00000496822.1:p.Ala307=
ENST00000648381.1:n.1088C=
ENST00000648853.1:c.878C=	ENSP00000497262.1:p.Ala293=
ENST00000649103.1:c.1019C=	ENSP00000497962.1:n.1019C=
ENST00000650591.1:c.1016C=	ENSP00000497376.1:p.Ala339=
ENST00000394236.7:c.920C=	ENSP00000377783.3:p.Ala307=
ENST00000407433.5:c.527C=	ENSP00000385794.1:p.Ala176=
NM_000313.3:c.920C= , LRG_572t1:c.920C=	NP_000304.2:p.Ala307=
NM_001314077.1:c.1016C= , LRG_572t2:c.1016C=	NP_001301006.1:p.Ala339=
NM_000313.4:c.920C= MANE Select	NP_000304.2:p.Ala307=
NM_001314077.2:c.1016C=	NP_001301006.1:p.Ala339=