Canonical Allele Identifier: CA1385030631

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879263C= , CM000665.2:g.93879263C=	GRCh38
NC_000003.11:g.93598107C= , CM000665.1:g.93598107C=	GRCh37
NC_000003.10:g.95080797C=	NCBI36
NG_009813.1:g.99828G= , LRG_572:g.99828G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1544G=	ENSP00000330021.7:p.Arg515=
ENST00000394236.9:c.1544G= MANE Select	ENSP00000377783.3:p.Arg515=
ENST00000407433.6:c.1499G=	ENSP00000385794.2:p.Arg500=
ENST00000647936.1:c.1544G=	ENSP00000496822.1:p.Arg515=
ENST00000648381.1:n.1712G=
ENST00000648853.1:c.1502G=	ENSP00000497262.1:p.Arg501=
ENST00000649103.1:c.1643G=	ENSP00000497962.1:n.1643G=
ENST00000649585.1:c.487G=	ENSP00000498163.1:n.487G=
ENST00000650591.1:c.1640G=	ENSP00000497376.1:p.Arg547=
ENST00000394236.7:c.1544G=	ENSP00000377783.3:p.Arg515=
ENST00000407433.5:c.1151G=	ENSP00000385794.1:p.Arg384=
NM_000313.3:c.1544G= , LRG_572t1:c.1544G=	NP_000304.2:p.Arg515=
NM_001314077.1:c.1640G= , LRG_572t2:c.1640G=	NP_001301006.1:p.Arg547=
NM_000313.4:c.1544G= MANE Select	NP_000304.2:p.Arg515=
NM_001314077.2:c.1640G=	NP_001301006.1:p.Arg547=