Canonical Allele Identifier: CA1385026921
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874309G= , CM000665.2:g.93874309G= GRCh38
NC_000003.11:g.93593153G= , CM000665.1:g.93593153G= GRCh37
NC_000003.10:g.95075843G= NCBI36
NG_009813.1:g.104782C= , LRG_572:g.104782C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1967C= ENSP00000330021.7:p.Ser656=
ENST00000394236.9:c.1967C= MANE Select ENSP00000377783.3:p.Ser656=
ENST00000407433.6:c.1922C= ENSP00000385794.2:p.Ser641=
ENST00000647936.1:c.*70C= ENSP00000496822.1:n.*70C=
ENST00000648381.1:n.2135C=
ENST00000648853.1:c.1925C= ENSP00000497262.1:p.Ser642=
ENST00000650591.1:c.2063C= ENSP00000497376.1:p.Ser688=
ENST00000394236.7:c.1967C= ENSP00000377783.3:p.Ser656=
ENST00000407433.5:c.1574C= ENSP00000385794.1:p.Ser525=
NM_000313.3:c.1967C= , LRG_572t1:c.1967C= NP_000304.2:p.Ser656=
NM_001314077.1:c.2063C= , LRG_572t2:c.2063C= NP_001301006.1:p.Ser688=
NM_000313.4:c.1967C= MANE Select NP_000304.2:p.Ser656=
NM_001314077.2:c.2063C= NP_001301006.1:p.Ser688=