Canonical Allele Identifier: CA1385029379
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877166G= , CM000665.2:g.93877166G= GRCh38
NC_000003.11:g.93596010G= , CM000665.1:g.93596010G= GRCh37
NC_000003.10:g.95078700G= NCBI36
NG_009813.1:g.101925C= , LRG_572:g.101925C=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1670C= ENSP00000330021.7:p.Thr557=
ENST00000394236.9:c.1670C= MANE Select ENSP00000377783.3:p.Thr557=
ENST00000407433.6:c.1625C= ENSP00000385794.2:p.Thr542=
ENST00000647936.1:c.1644+1997C= ENSP00000496822.1:n.1644+1997C=
ENST00000648381.1:n.1838C=
ENST00000648853.1:c.1628C= ENSP00000497262.1:p.Thr543=
ENST00000649103.1:c.1769C= ENSP00000497962.1:n.1769C=
ENST00000649585.1:c.613C= ENSP00000498163.1:n.613C=
ENST00000650591.1:c.1766C= ENSP00000497376.1:p.Thr589=
ENST00000394236.7:c.1670C= ENSP00000377783.3:p.Thr557=
ENST00000407433.5:c.1277C= ENSP00000385794.1:p.Thr426=
NM_000313.3:c.1670C= , LRG_572t1:c.1670C= NP_000304.2:p.Thr557=
NM_001314077.1:c.1766C= , LRG_572t2:c.1766C= NP_001301006.1:p.Thr589=
NM_000313.4:c.1670C= MANE Select NP_000304.2:p.Thr557=
NM_001314077.2:c.1766C= NP_001301006.1:p.Thr589=