Canonical Allele Identifier: CA1385028932

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877039G= , CM000665.2:g.93877039G=	GRCh38
NC_000003.11:g.93595883G= , CM000665.1:g.93595883G=	GRCh37
NC_000003.10:g.95078573G=	NCBI36
NG_009813.1:g.102052C= , LRG_572:g.102052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1797C=	ENSP00000330021.7:p.Asp599=
ENST00000394236.9:c.1797C= MANE Select	ENSP00000377783.3:p.Asp599=
ENST00000407433.6:c.1752C=	ENSP00000385794.2:p.Asp584=
ENST00000647936.1:c.1644+2124C=	ENSP00000496822.1:n.1644+2124C=
ENST00000648381.1:n.1965C=
ENST00000648853.1:c.1755C=	ENSP00000497262.1:p.Asp585=
ENST00000649585.1:c.740C=	ENSP00000498163.1:n.740C=
ENST00000650591.1:c.1893C=	ENSP00000497376.1:p.Asp631=
ENST00000394236.7:c.1797C=	ENSP00000377783.3:p.Asp599=
ENST00000407433.5:c.1404C=	ENSP00000385794.1:p.Asp468=
NM_000313.3:c.1797C= , LRG_572t1:c.1797C=	NP_000304.2:p.Asp599=
NM_001314077.1:c.1893C= , LRG_572t2:c.1893C=	NP_001301006.1:p.Asp631=
NM_000313.4:c.1797C= MANE Select	NP_000304.2:p.Asp599=
NM_001314077.2:c.1893C=	NP_001301006.1:p.Asp631=