Canonical Allele Identifier: CA1385039117

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898481T= , CM000665.2:g.93898481T=	GRCh38
NC_000003.11:g.93617325T= , CM000665.1:g.93617325T=	GRCh37
NC_000003.10:g.95100015T=	NCBI36
NG_009813.1:g.80610A= , LRG_572:g.80610A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.816A=	ENSP00000330021.7:p.Gly272=
ENST00000394236.9:c.816A= MANE Select	ENSP00000377783.3:p.Gly272=
ENST00000407433.6:c.771A=	ENSP00000385794.2:p.Gly257=
ENST00000647936.1:c.816A=	ENSP00000496822.1:p.Gly272=
ENST00000648381.1:n.984A=
ENST00000648853.1:c.774A=	ENSP00000497262.1:p.Gly258=
ENST00000649103.1:c.915A=	ENSP00000497962.1:n.915A=
ENST00000650591.1:c.912A=	ENSP00000497376.1:p.Gly304=
ENST00000394236.7:c.816A=	ENSP00000377783.3:p.Gly272=
ENST00000407433.5:c.423A=	ENSP00000385794.1:p.Gly141=
NM_000313.3:c.816A= , LRG_572t1:c.816A=	NP_000304.2:p.Gly272=
NM_001314077.1:c.912A= , LRG_572t2:c.912A=	NP_001301006.1:p.Gly304=
NM_000313.4:c.816A= MANE Select	NP_000304.2:p.Gly272=
NM_001314077.2:c.912A=	NP_001301006.1:p.Gly304=