Canonical Allele Identifier: CA1385033092

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93884869G= , CM000665.2:g.93884869G=	GRCh38
NC_000003.11:g.93603713G= , CM000665.1:g.93603713G=	GRCh37
NC_000003.10:g.95086403G=	NCBI36
NG_009813.1:g.94222C= , LRG_572:g.94222C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.1351C= MANE Select	NP_000304.2:p.Arg451=
ENST00000394236.9:c.1351C= MANE Select	ENSP00000377783.3:p.Arg451=
NM_000313.3:c.1351C= , LRG_572t1:c.1351C=	NP_000304.2:p.Arg451=
NM_001314077.1:c.1447C= , LRG_572t2:c.1447C=	NP_001301006.1:p.Arg483=
NM_001314077.2:c.1447C=	NP_001301006.1:p.Arg483=
ENST00000348974.5:c.1351C=	ENSP00000330021.7:p.Arg451=
ENST00000394236.7:c.1351C=	ENSP00000377783.3:p.Arg451=
ENST00000407433.5:c.958C=	ENSP00000385794.1:p.Arg320=
ENST00000407433.6:c.1306C=	ENSP00000385794.2:p.Arg436=
ENST00000647936.1:c.1351C=	ENSP00000496822.1:p.Arg451=
ENST00000648381.1:n.1519C=
ENST00000648853.1:c.1309C=	ENSP00000497262.1:p.Arg437=
ENST00000649103.1:c.1450C=	ENSP00000497962.1:n.1450C=
ENST00000649585.1:c.106C=	ENSP00000498163.1:p.Arg36=
ENST00000650591.1:c.1447C=	ENSP00000497376.1:p.Arg483=