Canonical Allele Identifier: CA1385026936

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874344A= , CM000665.2:g.93874344A=	GRCh38
NC_000003.11:g.93593188A= , CM000665.1:g.93593188A=	GRCh37
NC_000003.10:g.95075878A=	NCBI36
NG_009813.1:g.104747T= , LRG_572:g.104747T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1932T=	ENSP00000330021.7:p.Ile644=
ENST00000394236.9:c.1932T= MANE Select	ENSP00000377783.3:p.Ile644=
ENST00000407433.6:c.1887T=	ENSP00000385794.2:p.Ile629=
ENST00000647936.1:c.*35T=	ENSP00000496822.1:n.*35T=
ENST00000648381.1:n.2100T=
ENST00000648853.1:c.1890T=	ENSP00000497262.1:p.Ile630=
ENST00000650591.1:c.2028T=	ENSP00000497376.1:p.Ile676=
ENST00000394236.7:c.1932T=	ENSP00000377783.3:p.Ile644=
ENST00000407433.5:c.1539T=	ENSP00000385794.1:p.Ile513=
NM_000313.3:c.1932T= , LRG_572t1:c.1932T=	NP_000304.2:p.Ile644=
NM_001314077.1:c.2028T= , LRG_572t2:c.2028T=	NP_001301006.1:p.Ile676=
NM_000313.4:c.1932T= MANE Select	NP_000304.2:p.Ile644=
NM_001314077.2:c.2028T=	NP_001301006.1:p.Ile676=