Canonical Allele Identifier: CA1385039048

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898313A= , CM000665.2:g.93898313A=	GRCh38
NC_000003.11:g.93617157A= , CM000665.1:g.93617157A=	GRCh37
NC_000003.10:g.95099847A=	NCBI36
NG_009813.1:g.80778T= , LRG_572:g.80778T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.849+135T=	ENSP00000330021.7:n.849+135T=
ENST00000394236.9:c.849+135T= MANE Select	ENSP00000377783.3:n.849+135T=
ENST00000407433.6:c.804+135T=	ENSP00000385794.2:n.804+135T=
ENST00000647936.1:c.849+135T=	ENSP00000496822.1:n.849+135T=
ENST00000648381.1:n.1017+135T=
ENST00000648853.1:c.807+135T=	ENSP00000497262.1:n.807+135T=
ENST00000649103.1:c.948+135T=	ENSP00000497962.1:n.948+135T=
ENST00000650591.1:c.945+135T=	ENSP00000497376.1:n.945+135T=
ENST00000394236.7:c.849+135T=	ENSP00000377783.3:n.849+135T=
ENST00000407433.5:c.456+135T=	ENSP00000385794.1:n.456+135T=
NM_000313.3:c.849+135T= , LRG_572t1:c.849+135T=	NP_000304.2:n.849+135T=
NM_001314077.1:c.945+135T= , LRG_572t2:c.945+135T=	NP_001301006.1:n.945+135T=
NM_000313.4:c.849+135T= MANE Select	NP_000304.2:n.849+135T=
NM_001314077.2:c.945+135T=	NP_001301006.1:n.945+135T=