Canonical Allele Identifier: CA1385026941
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874355C= , CM000665.2:g.93874355C= GRCh38
NC_000003.11:g.93593199C= , CM000665.1:g.93593199C= GRCh37
NC_000003.10:g.95075889C= NCBI36
NG_009813.1:g.104736G= , LRG_572:g.104736G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1921G= ENSP00000330021.7:p.Glu641=
ENST00000394236.9:c.1921G= MANE Select ENSP00000377783.3:p.Glu641=
ENST00000407433.6:c.1876G= ENSP00000385794.2:p.Glu626=
ENST00000647936.1:c.*24G= ENSP00000496822.1:n.*24G=
ENST00000648381.1:n.2089G=
ENST00000648853.1:c.1879G= ENSP00000497262.1:p.Glu627=
ENST00000650591.1:c.2017G= ENSP00000497376.1:p.Glu673=
ENST00000394236.7:c.1921G= ENSP00000377783.3:p.Glu641=
ENST00000407433.5:c.1528G= ENSP00000385794.1:p.Glu510=
NM_000313.3:c.1921G= , LRG_572t1:c.1921G= NP_000304.2:p.Glu641=
NM_001314077.1:c.2017G= , LRG_572t2:c.2017G= NP_001301006.1:p.Glu673=
NM_000313.4:c.1921G= MANE Select NP_000304.2:p.Glu641=
NM_001314077.2:c.2017G= NP_001301006.1:p.Glu673=