Canonical Allele Identifier: CA1385059381

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927313T= , CM000665.2:g.93927313T=	GRCh38
NC_000003.11:g.93646157T= , CM000665.1:g.93646157T=	GRCh37
NC_000003.10:g.95128847T=	NCBI36
NG_009813.1:g.51778A= , LRG_572:g.51778A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.171A=	ENSP00000330021.7:p.Glu57=
ENST00000394236.9:c.171A= MANE Select	ENSP00000377783.3:p.Glu57=
ENST00000407433.6:c.171A=	ENSP00000385794.2:p.Glu57=
ENST00000472684.2:c.-223A=	ENSP00000419616.2:n.-223A=
ENST00000647936.1:c.171A=	ENSP00000496822.1:p.Glu57=
ENST00000648381.1:n.339A=
ENST00000648853.1:c.129A=	ENSP00000497262.1:p.Glu43=
ENST00000649103.1:c.150A=	ENSP00000497962.1:p.Glu50=
ENST00000650591.1:c.267A=	ENSP00000497376.1:p.Glu89=
ENST00000348974.4:c.267A=	ENSP00000330021.6:p.Glu89=
ENST00000394236.7:c.171A=	ENSP00000377783.3:p.Glu57=
ENST00000407433.5:c.-223A=	ENSP00000385794.1:n.-223A=
ENST00000472684.1:c.-223A=	ENSP00000419616.1:n.-223A=
NM_000313.3:c.171A= , LRG_572t1:c.171A=	NP_000304.2:p.Glu57=
NM_001314077.1:c.267A= , LRG_572t2:c.267A=	NP_001301006.1:p.Glu89=
NM_000313.4:c.171A= MANE Select	NP_000304.2:p.Glu57=
NM_001314077.2:c.267A=	NP_001301006.1:p.Glu89=