Canonical Allele Identifier: CA1385030600

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879187C= , CM000665.2:g.93879187C=	GRCh38
NC_000003.11:g.93598031C= , CM000665.1:g.93598031C=	GRCh37
NC_000003.10:g.95080721C=	NCBI36
NG_009813.1:g.99904G= , LRG_572:g.99904G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1620G=	ENSP00000330021.7:p.Val540=
ENST00000394236.9:c.1620G= MANE Select	ENSP00000377783.3:p.Val540=
ENST00000407433.6:c.1575G=	ENSP00000385794.2:p.Val525=
ENST00000647936.1:c.1620G=	ENSP00000496822.1:p.Val540=
ENST00000648381.1:n.1788G=
ENST00000648853.1:c.1578G=	ENSP00000497262.1:p.Val526=
ENST00000649103.1:c.1719G=	ENSP00000497962.1:n.1719G=
ENST00000649585.1:c.563G=	ENSP00000498163.1:n.563G=
ENST00000650591.1:c.1716G=	ENSP00000497376.1:p.Val572=
ENST00000394236.7:c.1620G=	ENSP00000377783.3:p.Val540=
ENST00000407433.5:c.1227G=	ENSP00000385794.1:p.Val409=
NM_000313.3:c.1620G= , LRG_572t1:c.1620G=	NP_000304.2:p.Val540=
NM_001314077.1:c.1716G= , LRG_572t2:c.1716G=	NP_001301006.1:p.Val572=
NM_000313.4:c.1620G= MANE Select	NP_000304.2:p.Val540=
NM_001314077.2:c.1716G=	NP_001301006.1:p.Val572=