Canonical Allele Identifier: CA1385033057

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93884775C= , CM000665.2:g.93884775C=	GRCh38
NC_000003.11:g.93603619C= , CM000665.1:g.93603619C=	GRCh37
NC_000003.10:g.95086309C=	NCBI36
NG_009813.1:g.94316G= , LRG_572:g.94316G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1445G=	ENSP00000330021.7:p.Gly482=
ENST00000394236.9:c.1445G= MANE Select	ENSP00000377783.3:p.Gly482=
ENST00000407433.6:c.1400G=	ENSP00000385794.2:p.Gly467=
ENST00000647936.1:c.1445G=	ENSP00000496822.1:p.Gly482=
ENST00000648381.1:n.1613G=
ENST00000648853.1:c.1403G=	ENSP00000497262.1:p.Gly468=
ENST00000649103.1:c.1544G=	ENSP00000497962.1:n.1544G=
ENST00000649585.1:c.200G=	ENSP00000498163.1:p.Gly67=
ENST00000650591.1:c.1541G=	ENSP00000497376.1:p.Gly514=
ENST00000394236.7:c.1445G=	ENSP00000377783.3:p.Gly482=
ENST00000407433.5:c.1052G=	ENSP00000385794.1:p.Gly351=
NM_000313.3:c.1445G= , LRG_572t1:c.1445G=	NP_000304.2:p.Gly482=
NM_001314077.1:c.1541G= , LRG_572t2:c.1541G=	NP_001301006.1:p.Gly514=
NM_000313.4:c.1445G= MANE Select	NP_000304.2:p.Gly482=
NM_001314077.2:c.1541G=	NP_001301006.1:p.Gly514=