Canonical Allele Identifier: CA1385030626

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879251C= , CM000665.2:g.93879251C=	GRCh38
NC_000003.11:g.93598095C= , CM000665.1:g.93598095C=	GRCh37
NC_000003.10:g.95080785C=	NCBI36
NG_009813.1:g.99840G= , LRG_572:g.99840G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1556G=	ENSP00000330021.7:p.Gly519=
ENST00000394236.9:c.1556G= MANE Select	ENSP00000377783.3:p.Gly519=
ENST00000407433.6:c.1511G=	ENSP00000385794.2:p.Gly504=
ENST00000647936.1:c.1556G=	ENSP00000496822.1:p.Gly519=
ENST00000648381.1:n.1724G=
ENST00000648853.1:c.1514G=	ENSP00000497262.1:p.Gly505=
ENST00000649103.1:c.1655G=	ENSP00000497962.1:n.1655G=
ENST00000649585.1:c.499G=	ENSP00000498163.1:n.499G=
ENST00000650591.1:c.1652G=	ENSP00000497376.1:p.Gly551=
ENST00000394236.7:c.1556G=	ENSP00000377783.3:p.Gly519=
ENST00000407433.5:c.1163G=	ENSP00000385794.1:p.Gly388=
NM_000313.3:c.1556G= , LRG_572t1:c.1556G=	NP_000304.2:p.Gly519=
NM_001314077.1:c.1652G= , LRG_572t2:c.1652G=	NP_001301006.1:p.Gly551=
NM_000313.4:c.1556G= MANE Select	NP_000304.2:p.Gly519=
NM_001314077.2:c.1652G=	NP_001301006.1:p.Gly551=