Canonical Allele Identifier: CA1385040189

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900830T= , CM000665.2:g.93900830T=	GRCh38
NC_000003.11:g.93619674T= , CM000665.1:g.93619674T=	GRCh37
NC_000003.10:g.95102364T=	NCBI36
NG_009813.1:g.78261A= , LRG_572:g.78261A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.701A=	ENSP00000330021.7:p.Tyr234=
ENST00000394236.9:c.701A= MANE Select	ENSP00000377783.3:p.Tyr234=
ENST00000407433.6:c.656A=	ENSP00000385794.2:p.Tyr219=
ENST00000647936.1:c.701A=	ENSP00000496822.1:p.Tyr234=
ENST00000648381.1:n.869A=
ENST00000648853.1:c.659A=	ENSP00000497262.1:p.Tyr220=
ENST00000649103.1:c.800A=	ENSP00000497962.1:n.800A=
ENST00000650591.1:c.797A=	ENSP00000497376.1:p.Tyr266=
ENST00000394236.7:c.701A=	ENSP00000377783.3:p.Tyr234=
ENST00000407433.5:c.308A=	ENSP00000385794.1:p.Tyr103=
NM_000313.3:c.701A= , LRG_572t1:c.701A=	NP_000304.2:p.Tyr234=
NM_001314077.1:c.797A= , LRG_572t2:c.797A=	NP_001301006.1:p.Tyr266=
NM_000313.4:c.701A= MANE Select	NP_000304.2:p.Tyr234=
NM_001314077.2:c.797A=	NP_001301006.1:p.Tyr266=