Canonical Allele Identifier: CA3099644260

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893121A= , CM000665.2:g.93893121A=	GRCh38
NC_000003.11:g.93611965A= , CM000665.1:g.93611965A=	GRCh37
NC_000003.10:g.95094655A=	NCBI36
NG_009813.1:g.85970T= , LRG_572:g.85970T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.967T= MANE Select	NP_000304.2:p.Phe323=
ENST00000394236.9:c.967T= MANE Select	ENSP00000377783.3:p.Phe323=
NM_000313.3:c.967T= , LRG_572t1:c.967T=	NP_000304.2:p.Phe323=
NM_001314077.1:c.1063T= , LRG_572t2:c.1063T=	NP_001301006.1:p.Phe355=
NM_001314077.2:c.1063T=	NP_001301006.1:p.Phe355=
ENST00000348974.5:c.967T=	ENSP00000330021.7:p.Phe323=
ENST00000394236.7:c.967T=	ENSP00000377783.3:p.Phe323=
ENST00000407433.5:c.574T=	ENSP00000385794.1:p.Phe192=
ENST00000407433.6:c.922T=	ENSP00000385794.2:p.Phe308=
ENST00000647936.1:c.967T=	ENSP00000496822.1:p.Phe323=
ENST00000648381.1:n.1135T=
ENST00000648853.1:c.925T=	ENSP00000497262.1:p.Phe309=
ENST00000649103.1:c.1066T=	ENSP00000497962.1:n.1066T=
ENST00000650591.1:c.1063T=	ENSP00000497376.1:p.Phe355=