Canonical Allele Identifier: CA1385030633

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879267T= , CM000665.2:g.93879267T=	GRCh38
NC_000003.11:g.93598111T= , CM000665.1:g.93598111T=	GRCh37
NC_000003.10:g.95080801T=	NCBI36
NG_009813.1:g.99824A= , LRG_572:g.99824A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1540A=	ENSP00000330021.7:p.Ile514=
ENST00000394236.9:c.1540A= MANE Select	ENSP00000377783.3:p.Ile514=
ENST00000407433.6:c.1495A=	ENSP00000385794.2:p.Ile499=
ENST00000647936.1:c.1540A=	ENSP00000496822.1:p.Ile514=
ENST00000648381.1:n.1708A=
ENST00000648853.1:c.1498A=	ENSP00000497262.1:p.Ile500=
ENST00000649103.1:c.1639A=	ENSP00000497962.1:n.1639A=
ENST00000649585.1:c.483A=	ENSP00000498163.1:n.483A=
ENST00000650591.1:c.1636A=	ENSP00000497376.1:p.Ile546=
ENST00000394236.7:c.1540A=	ENSP00000377783.3:p.Ile514=
ENST00000407433.5:c.1147A=	ENSP00000385794.1:p.Ile383=
NM_000313.3:c.1540A= , LRG_572t1:c.1540A=	NP_000304.2:p.Ile514=
NM_001314077.1:c.1636A= , LRG_572t2:c.1636A=	NP_001301006.1:p.Ile546=
NM_000313.4:c.1540A= MANE Select	NP_000304.2:p.Ile514=
NM_001314077.2:c.1636A=	NP_001301006.1:p.Ile546=