Canonical Allele Identifier: CA1385030642

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879288G= , CM000665.2:g.93879288G=	GRCh38
NC_000003.11:g.93598132G= , CM000665.1:g.93598132G=	GRCh37
NC_000003.10:g.95080822G=	NCBI36
NG_009813.1:g.99803C= , LRG_572:g.99803C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1519C=	ENSP00000330021.7:p.His507=
ENST00000394236.9:c.1519C= MANE Select	ENSP00000377783.3:p.His507=
ENST00000407433.6:c.1474C=	ENSP00000385794.2:p.His492=
ENST00000647936.1:c.1519C=	ENSP00000496822.1:p.His507=
ENST00000648381.1:n.1687C=
ENST00000648853.1:c.1477C=	ENSP00000497262.1:p.His493=
ENST00000649103.1:c.1618C=	ENSP00000497962.1:n.1618C=
ENST00000649585.1:c.462C=	ENSP00000498163.1:n.462C=
ENST00000650591.1:c.1615C=	ENSP00000497376.1:p.His539=
ENST00000394236.7:c.1519C=	ENSP00000377783.3:p.His507=
ENST00000407433.5:c.1126C=	ENSP00000385794.1:p.His376=
NM_000313.3:c.1519C= , LRG_572t1:c.1519C=	NP_000304.2:p.His507=
NM_001314077.1:c.1615C= , LRG_572t2:c.1615C=	NP_001301006.1:p.His539=
NM_000313.4:c.1519C= MANE Select	NP_000304.2:p.His507=
NM_001314077.2:c.1615C=	NP_001301006.1:p.His539=