Canonical Allele Identifier: CA1385040177

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900814C= , CM000665.2:g.93900814C=	GRCh38
NC_000003.11:g.93619658C= , CM000665.1:g.93619658C=	GRCh37
NC_000003.10:g.95102348C=	NCBI36
NG_009813.1:g.78277G= , LRG_572:g.78277G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.717G=	ENSP00000330021.7:p.Lys239=
ENST00000394236.9:c.717G= MANE Select	ENSP00000377783.3:p.Lys239=
ENST00000407433.6:c.672G=	ENSP00000385794.2:p.Lys224=
ENST00000647936.1:c.717G=	ENSP00000496822.1:p.Lys239=
ENST00000648381.1:n.885G=
ENST00000648853.1:c.675G=	ENSP00000497262.1:p.Lys225=
ENST00000649103.1:c.816G=	ENSP00000497962.1:n.816G=
ENST00000650591.1:c.813G=	ENSP00000497376.1:p.Lys271=
ENST00000394236.7:c.717G=	ENSP00000377783.3:p.Lys239=
ENST00000407433.5:c.324G=	ENSP00000385794.1:p.Lys108=
NM_000313.3:c.717G= , LRG_572t1:c.717G=	NP_000304.2:p.Lys239=
NM_001314077.1:c.813G= , LRG_572t2:c.813G=	NP_001301006.1:p.Lys271=
NM_000313.4:c.717G= MANE Select	NP_000304.2:p.Lys239=
NM_001314077.2:c.813G=	NP_001301006.1:p.Lys271=