Canonical Allele Identifier: CA1385059258

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927251G= , CM000665.2:g.93927251G=	GRCh38
NC_000003.11:g.93646095G= , CM000665.1:g.93646095G=	GRCh37
NC_000003.10:g.95128785G=	NCBI36
NG_009813.1:g.51840C= , LRG_572:g.51840C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000313.4:c.233C= MANE Select	NP_000304.2:p.Thr78=
ENST00000394236.9:c.233C= MANE Select	ENSP00000377783.3:p.Thr78=
NM_000313.3:c.233C= , LRG_572t1:c.233C=	NP_000304.2:p.Thr78=
NM_001314077.1:c.329C= , LRG_572t2:c.329C=	NP_001301006.1:p.Thr110=
NM_001314077.2:c.329C=	NP_001301006.1:p.Thr110=
ENST00000348974.4:c.329C=	ENSP00000330021.6:p.Thr110=
ENST00000348974.5:c.233C=	ENSP00000330021.7:p.Thr78=
ENST00000394236.7:c.233C=	ENSP00000377783.3:p.Thr78=
ENST00000407433.5:c.-161C=	ENSP00000385794.1:n.-161C=
ENST00000407433.6:c.233C=	ENSP00000385794.2:p.Thr78=
ENST00000472684.1:c.-161C=	ENSP00000419616.1:n.-161C=
ENST00000472684.2:c.-161C=	ENSP00000419616.2:n.-161C=
ENST00000647936.1:c.233C=	ENSP00000496822.1:p.Thr78=
ENST00000648381.1:n.401C=
ENST00000648853.1:c.191C=	ENSP00000497262.1:p.Thr64=
ENST00000649103.1:c.212C=	ENSP00000497962.1:p.Thr71=
ENST00000650591.1:c.329C=	ENSP00000497376.1:p.Thr110=