Canonical Allele Identifier: CA1385038297

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896592A= , CM000665.2:g.93896592A=	GRCh38
NC_000003.11:g.93615436A= , CM000665.1:g.93615436A=	GRCh37
NC_000003.10:g.95098126A=	NCBI36
NG_009813.1:g.82499T= , LRG_572:g.82499T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.949T=	ENSP00000330021.7:p.Leu317=
ENST00000394236.9:c.949T= MANE Select	ENSP00000377783.3:p.Leu317=
ENST00000407433.6:c.904T=	ENSP00000385794.2:p.Leu302=
ENST00000647936.1:c.949T=	ENSP00000496822.1:p.Leu317=
ENST00000648381.1:n.1117T=
ENST00000648853.1:c.907T=	ENSP00000497262.1:p.Leu303=
ENST00000649103.1:c.1048T=	ENSP00000497962.1:n.1048T=
ENST00000650591.1:c.1045T=	ENSP00000497376.1:p.Leu349=
ENST00000394236.7:c.949T=	ENSP00000377783.3:p.Leu317=
ENST00000407433.5:c.556T=	ENSP00000385794.1:p.Leu186=
NM_000313.3:c.949T= , LRG_572t1:c.949T=	NP_000304.2:p.Leu317=
NM_001314077.1:c.1045T= , LRG_572t2:c.1045T=	NP_001301006.1:p.Leu349=
NM_000313.4:c.949T= MANE Select	NP_000304.2:p.Leu317=
NM_001314077.2:c.1045T=	NP_001301006.1:p.Leu349=