Canonical Allele Identifier: CA1385042620

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905889T= , CM000665.2:g.93905889T=	GRCh38
NC_000003.11:g.93624733T= , CM000665.1:g.93624733T=	GRCh37
NC_000003.10:g.95107423T=	NCBI36
NG_009813.1:g.73202A= , LRG_572:g.73202A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.496A=	ENSP00000330021.7:p.Asn166=
ENST00000394236.9:c.496A= MANE Select	ENSP00000377783.3:p.Asn166=
ENST00000407433.6:c.496A=	ENSP00000385794.2:p.Asn166=
ENST00000472684.2:c.103A=	ENSP00000419616.2:p.Asn35=
ENST00000647936.1:c.496A=	ENSP00000496822.1:p.Asn166=
ENST00000648381.1:n.664A=
ENST00000648853.1:c.454A=	ENSP00000497262.1:p.Asn152=
ENST00000649103.1:c.595A=	ENSP00000497962.1:n.595A=
ENST00000650591.1:c.592A=	ENSP00000497376.1:p.Asn198=
ENST00000348974.4:c.592A=	ENSP00000330021.6:p.Asn198=
ENST00000394236.7:c.496A=	ENSP00000377783.3:p.Asn166=
ENST00000407433.5:c.103A=	ENSP00000385794.1:p.Asn35=
ENST00000472684.1:c.103A=	ENSP00000419616.1:p.Asn35=
NM_000313.3:c.496A= , LRG_572t1:c.496A=	NP_000304.2:p.Asn166=
NM_001314077.1:c.592A= , LRG_572t2:c.592A=	NP_001301006.1:p.Asn198=
NM_000313.4:c.496A= MANE Select	NP_000304.2:p.Asn166=
NM_001314077.2:c.592A=	NP_001301006.1:p.Asn198=