Canonical Allele Identifier: CA1385038316

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896628G= , CM000665.2:g.93896628G=	GRCh38
NC_000003.11:g.93615472G= , CM000665.1:g.93615472G=	GRCh37
NC_000003.10:g.95098162G=	NCBI36
NG_009813.1:g.82463C= , LRG_572:g.82463C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.913C=	ENSP00000330021.7:p.Gln305=
ENST00000394236.9:c.913C= MANE Select	ENSP00000377783.3:p.Gln305=
ENST00000407433.6:c.868C=	ENSP00000385794.2:p.Gln290=
ENST00000647936.1:c.913C=	ENSP00000496822.1:p.Gln305=
ENST00000648381.1:n.1081C=
ENST00000648853.1:c.871C=	ENSP00000497262.1:p.Gln291=
ENST00000649103.1:c.1012C=	ENSP00000497962.1:n.1012C=
ENST00000650591.1:c.1009C=	ENSP00000497376.1:p.Gln337=
ENST00000394236.7:c.913C=	ENSP00000377783.3:p.Gln305=
ENST00000407433.5:c.520C=	ENSP00000385794.1:p.Gln174=
NM_000313.3:c.913C= , LRG_572t1:c.913C=	NP_000304.2:p.Gln305=
NM_001314077.1:c.1009C= , LRG_572t2:c.1009C=	NP_001301006.1:p.Gln337=
NM_000313.4:c.913C= MANE Select	NP_000304.2:p.Gln305=
NM_001314077.2:c.1009C=	NP_001301006.1:p.Gln337=