Canonical Allele Identifier: CA1385026909
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874280A= , CM000665.2:g.93874280A= GRCh38
NC_000003.11:g.93593124A= , CM000665.1:g.93593124A= GRCh37
NC_000003.10:g.95075814A= NCBI36
NG_009813.1:g.104811T= , LRG_572:g.104811T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1996T= ENSP00000330021.7:p.Cys666=
ENST00000394236.9:c.1996T= MANE Select ENSP00000377783.3:p.Cys666=
ENST00000407433.6:c.1951T= ENSP00000385794.2:p.Cys651=
ENST00000647936.1:c.*99T= ENSP00000496822.1:n.*99T=
ENST00000648381.1:n.2164T=
ENST00000648853.1:c.1954T= ENSP00000497262.1:p.Cys652=
ENST00000650591.1:c.2092T= ENSP00000497376.1:p.Cys698=
ENST00000394236.7:c.1996T= ENSP00000377783.3:p.Cys666=
ENST00000407433.5:c.1603T= ENSP00000385794.1:p.Cys535=
NM_000313.3:c.1996T= , LRG_572t1:c.1996T= NP_000304.2:p.Cys666=
NM_001314077.1:c.2092T= , LRG_572t2:c.2092T= NP_001301006.1:p.Cys698=
NM_000313.4:c.1996T= MANE Select NP_000304.2:p.Cys666=
NM_001314077.2:c.2092T= NP_001301006.1:p.Cys698=