Canonical Allele Identifier: CA1385028861

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93876990C= , CM000665.2:g.93876990C=	GRCh38
NC_000003.11:g.93595834C= , CM000665.1:g.93595834C=	GRCh37
NC_000003.10:g.95078524C=	NCBI36
NG_009813.1:g.102101G= , LRG_572:g.102101G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1846G=	ENSP00000330021.7:p.Ala616=
ENST00000394236.9:c.1846G= MANE Select	ENSP00000377783.3:p.Ala616=
ENST00000407433.6:c.1801G=	ENSP00000385794.2:p.Ala601=
ENST00000647936.1:c.1644+2173G=	ENSP00000496822.1:n.1644+2173G=
ENST00000648381.1:n.2014G=
ENST00000648853.1:c.1804G=	ENSP00000497262.1:p.Ala602=
ENST00000650591.1:c.1942G=	ENSP00000497376.1:p.Ala648=
ENST00000394236.7:c.1846G=	ENSP00000377783.3:p.Ala616=
ENST00000407433.5:c.1453G=	ENSP00000385794.1:p.Ala485=
NM_000313.3:c.1846G= , LRG_572t1:c.1846G=	NP_000304.2:p.Ala616=
NM_001314077.1:c.1942G= , LRG_572t2:c.1942G=	NP_001301006.1:p.Ala648=
NM_000313.4:c.1846G= MANE Select	NP_000304.2:p.Ala616=
NM_001314077.2:c.1942G=	NP_001301006.1:p.Ala648=