Canonical Allele Identifier: CA1385026905

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874275T= , CM000665.2:g.93874275T=	GRCh38
NC_000003.11:g.93593119T= , CM000665.1:g.93593119T=	GRCh37
NC_000003.10:g.95075809T=	NCBI36
NG_009813.1:g.104816A= , LRG_572:g.104816A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.2001A=	ENSP00000330021.7:p.Pro667=
ENST00000394236.9:c.2001A= MANE Select	ENSP00000377783.3:p.Pro667=
ENST00000407433.6:c.1956A=	ENSP00000385794.2:p.Pro652=
ENST00000647936.1:c.*104A=	ENSP00000496822.1:n.*104A=
ENST00000648381.1:n.2169A=
ENST00000648853.1:c.1959A=	ENSP00000497262.1:p.Pro653=
ENST00000650591.1:c.2097A=	ENSP00000497376.1:p.Pro699=
ENST00000394236.7:c.2001A=	ENSP00000377783.3:p.Pro667=
ENST00000407433.5:c.1608A=	ENSP00000385794.1:p.Pro536=
NM_000313.3:c.2001A= , LRG_572t1:c.2001A=	NP_000304.2:p.Pro667=
NM_001314077.1:c.2097A= , LRG_572t2:c.2097A=	NP_001301006.1:p.Pro699=
NM_000313.4:c.2001A= MANE Select	NP_000304.2:p.Pro667=
NM_001314077.2:c.2097A=	NP_001301006.1:p.Pro699=