Canonical Allele Identifier: CA1385040196

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900844G= , CM000665.2:g.93900844G=	GRCh38
NC_000003.11:g.93619688G= , CM000665.1:g.93619688G=	GRCh37
NC_000003.10:g.95102378G=	NCBI36
NG_009813.1:g.78247C= , LRG_572:g.78247C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.687C=	ENSP00000330021.7:p.Pro229=
ENST00000394236.9:c.687C= MANE Select	ENSP00000377783.3:p.Pro229=
ENST00000407433.6:c.642C=	ENSP00000385794.2:p.Pro214=
ENST00000647936.1:c.687C=	ENSP00000496822.1:p.Pro229=
ENST00000648381.1:n.855C=
ENST00000648853.1:c.645C=	ENSP00000497262.1:p.Pro215=
ENST00000649103.1:c.786C=	ENSP00000497962.1:n.786C=
ENST00000650591.1:c.783C=	ENSP00000497376.1:p.Pro261=
ENST00000394236.7:c.687C=	ENSP00000377783.3:p.Pro229=
ENST00000407433.5:c.294C=	ENSP00000385794.1:p.Pro98=
NM_000313.3:c.687C= , LRG_572t1:c.687C=	NP_000304.2:p.Pro229=
NM_001314077.1:c.783C= , LRG_572t2:c.783C=	NP_001301006.1:p.Pro261=
NM_000313.4:c.687C= MANE Select	NP_000304.2:p.Pro229=
NM_001314077.2:c.783C=	NP_001301006.1:p.Pro261=