Canonical Allele Identifier: CA1385028885

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877006T= , CM000665.2:g.93877006T=	GRCh38
NC_000003.11:g.93595850T= , CM000665.1:g.93595850T=	GRCh37
NC_000003.10:g.95078540T=	NCBI36
NG_009813.1:g.102085A= , LRG_572:g.102085A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1830A=	ENSP00000330021.7:p.Ala610=
ENST00000394236.9:c.1830A= MANE Select	ENSP00000377783.3:p.Ala610=
ENST00000407433.6:c.1785A=	ENSP00000385794.2:p.Ala595=
ENST00000647936.1:c.1644+2157A=	ENSP00000496822.1:n.1644+2157A=
ENST00000648381.1:n.1998A=
ENST00000648853.1:c.1788A=	ENSP00000497262.1:p.Ala596=
ENST00000649585.1:c.773A=	ENSP00000498163.1:n.773A=
ENST00000650591.1:c.1926A=	ENSP00000497376.1:p.Ala642=
ENST00000394236.7:c.1830A=	ENSP00000377783.3:p.Ala610=
ENST00000407433.5:c.1437A=	ENSP00000385794.1:p.Ala479=
NM_000313.3:c.1830A= , LRG_572t1:c.1830A=	NP_000304.2:p.Ala610=
NM_001314077.1:c.1926A= , LRG_572t2:c.1926A=	NP_001301006.1:p.Ala642=
NM_000313.4:c.1830A= MANE Select	NP_000304.2:p.Ala610=
NM_001314077.2:c.1926A=	NP_001301006.1:p.Ala642=