Canonical Allele Identifier: CA1385040190

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900832T= , CM000665.2:g.93900832T=	GRCh38
NC_000003.11:g.93619676T= , CM000665.1:g.93619676T=	GRCh37
NC_000003.10:g.95102366T=	NCBI36
NG_009813.1:g.78259A= , LRG_572:g.78259A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.699A=	ENSP00000330021.7:p.Arg233=
ENST00000394236.9:c.699A= MANE Select	ENSP00000377783.3:p.Arg233=
ENST00000407433.6:c.654A=	ENSP00000385794.2:p.Arg218=
ENST00000647936.1:c.699A=	ENSP00000496822.1:p.Arg233=
ENST00000648381.1:n.867A=
ENST00000648853.1:c.657A=	ENSP00000497262.1:p.Arg219=
ENST00000649103.1:c.798A=	ENSP00000497962.1:n.798A=
ENST00000650591.1:c.795A=	ENSP00000497376.1:p.Arg265=
ENST00000394236.7:c.699A=	ENSP00000377783.3:p.Arg233=
ENST00000407433.5:c.306A=	ENSP00000385794.1:p.Arg102=
NM_000313.3:c.699A= , LRG_572t1:c.699A=	NP_000304.2:p.Arg233=
NM_001314077.1:c.795A= , LRG_572t2:c.795A=	NP_001301006.1:p.Arg265=
NM_000313.4:c.699A= MANE Select	NP_000304.2:p.Arg233=
NM_001314077.2:c.795A=	NP_001301006.1:p.Arg265=