Canonical Allele Identifier: CA1385030653

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879306A= , CM000665.2:g.93879306A=	GRCh38
NC_000003.11:g.93598150A= , CM000665.1:g.93598150A=	GRCh37
NC_000003.10:g.95080840A=	NCBI36
NG_009813.1:g.99785T= , LRG_572:g.99785T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.1501T= MANE Select	NP_000304.2:p.Ser501=
ENST00000394236.9:c.1501T= MANE Select	ENSP00000377783.3:p.Ser501=
NM_000313.3:c.1501T= , LRG_572t1:c.1501T=	NP_000304.2:p.Ser501=
NM_001314077.1:c.1597T= , LRG_572t2:c.1597T=	NP_001301006.1:p.Ser533=
NM_001314077.2:c.1597T=	NP_001301006.1:p.Ser533=
ENST00000348974.5:c.1501T=	ENSP00000330021.7:p.Ser501=
ENST00000394236.7:c.1501T=	ENSP00000377783.3:p.Ser501=
ENST00000407433.5:c.1108T=	ENSP00000385794.1:p.Ser370=
ENST00000407433.6:c.1456T=	ENSP00000385794.2:p.Ser486=
ENST00000647936.1:c.1501T=	ENSP00000496822.1:p.Ser501=
ENST00000648381.1:n.1669T=
ENST00000648853.1:c.1459T=	ENSP00000497262.1:p.Ser487=
ENST00000649103.1:c.1600T=	ENSP00000497962.1:n.1600T=
ENST00000649585.1:c.444T=	ENSP00000498163.1:n.444T=
ENST00000650591.1:c.1597T=	ENSP00000497376.1:p.Ser533=