Canonical Allele Identifier: CA1385033847

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93886430G= , CM000665.2:g.93886430G=	GRCh38
NC_000003.11:g.93605274G= , CM000665.1:g.93605274G=	GRCh37
NC_000003.10:g.95087964G=	NCBI36
NG_009813.1:g.92661C= , LRG_572:g.92661C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1229C=	ENSP00000330021.7:p.Pro410=
ENST00000394236.9:c.1229C= MANE Select	ENSP00000377783.3:p.Pro410=
ENST00000407433.6:c.1184C=	ENSP00000385794.2:p.Pro395=
ENST00000647936.1:c.1229C=	ENSP00000496822.1:p.Pro410=
ENST00000648381.1:n.1397C=
ENST00000648853.1:c.1187C=	ENSP00000497262.1:p.Pro396=
ENST00000649103.1:c.1328C=	ENSP00000497962.1:n.1328C=
ENST00000650591.1:c.1325C=	ENSP00000497376.1:p.Pro442=
ENST00000394236.7:c.1229C=	ENSP00000377783.3:p.Pro410=
ENST00000407433.5:c.836C=	ENSP00000385794.1:p.Pro279=
NM_000313.3:c.1229C= , LRG_572t1:c.1229C=	NP_000304.2:p.Pro410=
NM_001314077.1:c.1325C= , LRG_572t2:c.1325C=	NP_001301006.1:p.Pro442=
NM_000313.4:c.1229C= MANE Select	NP_000304.2:p.Pro410=
NM_001314077.2:c.1325C=	NP_001301006.1:p.Pro442=