Canonical Allele Identifier: CA1385038303

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896602T= , CM000665.2:g.93896602T=	GRCh38
NC_000003.11:g.93615446T= , CM000665.1:g.93615446T=	GRCh37
NC_000003.10:g.95098136T=	NCBI36
NG_009813.1:g.82489A= , LRG_572:g.82489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.939A=	ENSP00000330021.7:p.Leu313=
ENST00000394236.9:c.939A= MANE Select	ENSP00000377783.3:p.Leu313=
ENST00000407433.6:c.894A=	ENSP00000385794.2:p.Leu298=
ENST00000647936.1:c.939A=	ENSP00000496822.1:p.Leu313=
ENST00000648381.1:n.1107A=
ENST00000648853.1:c.897A=	ENSP00000497262.1:p.Leu299=
ENST00000649103.1:c.1038A=	ENSP00000497962.1:n.1038A=
ENST00000650591.1:c.1035A=	ENSP00000497376.1:p.Leu345=
ENST00000394236.7:c.939A=	ENSP00000377783.3:p.Leu313=
ENST00000407433.5:c.546A=	ENSP00000385794.1:p.Leu182=
NM_000313.3:c.939A= , LRG_572t1:c.939A=	NP_000304.2:p.Leu313=
NM_001314077.1:c.1035A= , LRG_572t2:c.1035A=	NP_001301006.1:p.Leu345=
NM_000313.4:c.939A= MANE Select	NP_000304.2:p.Leu313=
NM_001314077.2:c.1035A=	NP_001301006.1:p.Leu345=