Canonical Allele Identifier: CA1385039995

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900382A= , CM000665.2:g.93900382A=	GRCh38
NC_000003.11:g.93619226A= , CM000665.1:g.93619226A=	GRCh37
NC_000003.10:g.95101916A=	NCBI36
NG_009813.1:g.78709T= , LRG_572:g.78709T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+422T=	ENSP00000330021.7:n.727+422T=
ENST00000394236.9:c.727+422T= MANE Select	ENSP00000377783.3:n.727+422T=
ENST00000407433.6:c.682+422T=	ENSP00000385794.2:n.682+422T=
ENST00000647936.1:c.727+422T=	ENSP00000496822.1:n.727+422T=
ENST00000648381.1:n.895+422T=
ENST00000648853.1:c.685+422T=	ENSP00000497262.1:n.685+422T=
ENST00000649103.1:c.826+422T=	ENSP00000497962.1:n.826+422T=
ENST00000650591.1:c.823+422T=	ENSP00000497376.1:n.823+422T=
ENST00000394236.7:c.727+422T=	ENSP00000377783.3:n.727+422T=
ENST00000407433.5:c.334+422T=	ENSP00000385794.1:n.334+422T=
NM_000313.3:c.727+422T= , LRG_572t1:c.727+422T=	NP_000304.2:n.727+422T=
NM_001314077.1:c.823+422T= , LRG_572t2:c.823+422T=	NP_001301006.1:n.823+422T=
NM_000313.4:c.727+422T= MANE Select	NP_000304.2:n.727+422T=
NM_001314077.2:c.823+422T=	NP_001301006.1:n.823+422T=