Canonical Allele Identifier: CA1385044714

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93908918G= , CM000665.2:g.93908918G=	GRCh38
NC_000003.11:g.93627762G= , CM000665.1:g.93627762G=	GRCh37
NC_000003.10:g.95110452G=	NCBI36
NG_009813.1:g.70173C= , LRG_572:g.70173C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.346+1701C=	ENSP00000330021.7:n.346+1701C=
ENST00000394236.9:c.346+1701C= MANE Select	ENSP00000377783.3:n.346+1701C=
ENST00000407433.6:c.346+1701C=	ENSP00000385794.2:n.346+1701C=
ENST00000472684.2:c.-48+1701C=	ENSP00000419616.2:n.-48+1701C=
ENST00000647936.1:c.346+1701C=	ENSP00000496822.1:n.346+1701C=
ENST00000648381.1:n.514+1701C=
ENST00000648853.1:c.304+1701C=	ENSP00000497262.1:n.304+1701C=
ENST00000649103.1:c.445+1701C=	ENSP00000497962.1:n.445+1701C=
ENST00000650591.1:c.442+1701C=	ENSP00000497376.1:n.442+1701C=
ENST00000348974.4:c.442+1701C=	ENSP00000330021.6:n.442+1701C=
ENST00000394236.7:c.346+1701C=	ENSP00000377783.3:n.346+1701C=
ENST00000407433.5:c.-48+1701C=	ENSP00000385794.1:n.-48+1701C=
ENST00000472684.1:c.-48+1701C=	ENSP00000419616.1:n.-48+1701C=
ENST00000488658.1:n.539+1701C=
NM_000313.3:c.346+1701C= , LRG_572t1:c.346+1701C=	NP_000304.2:n.346+1701C=
NM_001314077.1:c.442+1701C= , LRG_572t2:c.442+1701C=	NP_001301006.1:n.442+1701C=
NM_000313.4:c.346+1701C= MANE Select	NP_000304.2:n.346+1701C=
NM_001314077.2:c.442+1701C=	NP_001301006.1:n.442+1701C=