Canonical Allele Identifier: CA1385040192

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900836T= , CM000665.2:g.93900836T=	GRCh38
NC_000003.11:g.93619680T= , CM000665.1:g.93619680T=	GRCh37
NC_000003.10:g.95102370T=	NCBI36
NG_009813.1:g.78255A= , LRG_572:g.78255A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.695A=	ENSP00000330021.7:p.Tyr232=
ENST00000394236.9:c.695A= MANE Select	ENSP00000377783.3:p.Tyr232=
ENST00000407433.6:c.650A=	ENSP00000385794.2:p.Tyr217=
ENST00000647936.1:c.695A=	ENSP00000496822.1:p.Tyr232=
ENST00000648381.1:n.863A=
ENST00000648853.1:c.653A=	ENSP00000497262.1:p.Tyr218=
ENST00000649103.1:c.794A=	ENSP00000497962.1:n.794A=
ENST00000650591.1:c.791A=	ENSP00000497376.1:p.Tyr264=
ENST00000394236.7:c.695A=	ENSP00000377783.3:p.Tyr232=
ENST00000407433.5:c.302A=	ENSP00000385794.1:p.Tyr101=
NM_000313.3:c.695A= , LRG_572t1:c.695A=	NP_000304.2:p.Tyr232=
NM_001314077.1:c.791A= , LRG_572t2:c.791A=	NP_001301006.1:p.Tyr264=
NM_000313.4:c.695A= MANE Select	NP_000304.2:p.Tyr232=
NM_001314077.2:c.791A=	NP_001301006.1:p.Tyr264=