Canonical Allele Identifier: CA1385040158

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900770T= , CM000665.2:g.93900770T=	GRCh38
NC_000003.11:g.93619614T= , CM000665.1:g.93619614T=	GRCh37
NC_000003.10:g.95102304T=	NCBI36
NG_009813.1:g.78321A= , LRG_572:g.78321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+34A=	ENSP00000330021.7:n.727+34A=
ENST00000394236.9:c.727+34A= MANE Select	ENSP00000377783.3:n.727+34A=
ENST00000407433.6:c.682+34A=	ENSP00000385794.2:n.682+34A=
ENST00000647936.1:c.727+34A=	ENSP00000496822.1:n.727+34A=
ENST00000648381.1:n.895+34A=
ENST00000648853.1:c.685+34A=	ENSP00000497262.1:n.685+34A=
ENST00000649103.1:c.826+34A=	ENSP00000497962.1:n.826+34A=
ENST00000650591.1:c.823+34A=	ENSP00000497376.1:n.823+34A=
ENST00000394236.7:c.727+34A=	ENSP00000377783.3:n.727+34A=
ENST00000407433.5:c.334+34A=	ENSP00000385794.1:n.334+34A=
NM_000313.3:c.727+34A= , LRG_572t1:c.727+34A=	NP_000304.2:n.727+34A=
NM_001314077.1:c.823+34A= , LRG_572t2:c.823+34A=	NP_001301006.1:n.823+34A=
NM_000313.4:c.727+34A= MANE Select	NP_000304.2:n.727+34A=
NM_001314077.2:c.823+34A=	NP_001301006.1:n.823+34A=