Canonical Allele Identifier: CA1385028927

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877029G= , CM000665.2:g.93877029G=	GRCh38
NC_000003.11:g.93595873G= , CM000665.1:g.93595873G=	GRCh37
NC_000003.10:g.95078563G=	NCBI36
NG_009813.1:g.102062C= , LRG_572:g.102062C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1807C=	ENSP00000330021.7:p.Gln603=
ENST00000394236.9:c.1807C= MANE Select	ENSP00000377783.3:p.Gln603=
ENST00000407433.6:c.1762C=	ENSP00000385794.2:p.Gln588=
ENST00000647936.1:c.1644+2134C=	ENSP00000496822.1:n.1644+2134C=
ENST00000648381.1:n.1975C=
ENST00000648853.1:c.1765C=	ENSP00000497262.1:p.Gln589=
ENST00000649585.1:c.750C=	ENSP00000498163.1:n.750C=
ENST00000650591.1:c.1903C=	ENSP00000497376.1:p.Gln635=
ENST00000394236.7:c.1807C=	ENSP00000377783.3:p.Gln603=
ENST00000407433.5:c.1414C=	ENSP00000385794.1:p.Gln472=
NM_000313.3:c.1807C= , LRG_572t1:c.1807C=	NP_000304.2:p.Gln603=
NM_001314077.1:c.1903C= , LRG_572t2:c.1903C=	NP_001301006.1:p.Gln635=
NM_000313.4:c.1807C= MANE Select	NP_000304.2:p.Gln603=
NM_001314077.2:c.1903C=	NP_001301006.1:p.Gln635=