Canonical Allele Identifier: CA1385059178

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927224A= , CM000665.2:g.93927224A=	GRCh38
NC_000003.11:g.93646068A= , CM000665.1:g.93646068A=	GRCh37
NC_000003.10:g.95128758A=	NCBI36
NG_009813.1:g.51867T= , LRG_572:g.51867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.234+26T=	ENSP00000330021.7:n.234+26T=
ENST00000394236.9:c.234+26T= MANE Select	ENSP00000377783.3:n.234+26T=
ENST00000407433.6:c.234+26T=	ENSP00000385794.2:n.234+26T=
ENST00000472684.2:c.-160+26T=	ENSP00000419616.2:n.-160+26T=
ENST00000647936.1:c.234+26T=	ENSP00000496822.1:n.234+26T=
ENST00000648381.1:n.402+26T=
ENST00000648853.1:c.192+26T=	ENSP00000497262.1:n.192+26T=
ENST00000649103.1:c.213+26T=	ENSP00000497962.1:n.213+26T=
ENST00000650591.1:c.330+26T=	ENSP00000497376.1:n.330+26T=
ENST00000348974.4:c.330+26T=	ENSP00000330021.6:n.330+26T=
ENST00000394236.7:c.234+26T=	ENSP00000377783.3:n.234+26T=
ENST00000407433.5:c.-160+26T=	ENSP00000385794.1:n.-160+26T=
ENST00000472684.1:c.-160+26T=	ENSP00000419616.1:n.-160+26T=
NM_000313.3:c.234+26T= , LRG_572t1:c.234+26T=	NP_000304.2:n.234+26T=
NM_001314077.1:c.330+26T= , LRG_572t2:c.330+26T=	NP_001301006.1:n.330+26T=
NM_000313.4:c.234+26T= MANE Select	NP_000304.2:n.234+26T=
NM_001314077.2:c.330+26T=	NP_001301006.1:n.330+26T=