Canonical Allele Identifier: CA1385040188

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900829A= , CM000665.2:g.93900829A=	GRCh38
NC_000003.11:g.93619673A= , CM000665.1:g.93619673A=	GRCh37
NC_000003.10:g.95102363A=	NCBI36
NG_009813.1:g.78262T= , LRG_572:g.78262T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.702T=	ENSP00000330021.7:p.Tyr234=
ENST00000394236.9:c.702T= MANE Select	ENSP00000377783.3:p.Tyr234=
ENST00000407433.6:c.657T=	ENSP00000385794.2:p.Tyr219=
ENST00000647936.1:c.702T=	ENSP00000496822.1:p.Tyr234=
ENST00000648381.1:n.870T=
ENST00000648853.1:c.660T=	ENSP00000497262.1:p.Tyr220=
ENST00000649103.1:c.801T=	ENSP00000497962.1:n.801T=
ENST00000650591.1:c.798T=	ENSP00000497376.1:p.Tyr266=
ENST00000394236.7:c.702T=	ENSP00000377783.3:p.Tyr234=
ENST00000407433.5:c.309T=	ENSP00000385794.1:p.Tyr103=
NM_000313.3:c.702T= , LRG_572t1:c.702T=	NP_000304.2:p.Tyr234=
NM_001314077.1:c.798T= , LRG_572t2:c.798T=	NP_001301006.1:p.Tyr266=
NM_000313.4:c.702T= MANE Select	NP_000304.2:p.Tyr234=
NM_001314077.2:c.798T=	NP_001301006.1:p.Tyr266=