Canonical Allele Identifier: CA1385026923
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874315G= , CM000665.2:g.93874315G= GRCh38
NC_000003.11:g.93593159G= , CM000665.1:g.93593159G= GRCh37
NC_000003.10:g.95075849G= NCBI36
NG_009813.1:g.104776C= , LRG_572:g.104776C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1961C= ENSP00000330021.7:p.Ala654=
ENST00000394236.9:c.1961C= MANE Select ENSP00000377783.3:p.Ala654=
ENST00000407433.6:c.1916C= ENSP00000385794.2:p.Ala639=
ENST00000647936.1:c.*64C= ENSP00000496822.1:n.*64C=
ENST00000648381.1:n.2129C=
ENST00000648853.1:c.1919C= ENSP00000497262.1:p.Ala640=
ENST00000650591.1:c.2057C= ENSP00000497376.1:p.Ala686=
ENST00000394236.7:c.1961C= ENSP00000377783.3:p.Ala654=
ENST00000407433.5:c.1568C= ENSP00000385794.1:p.Ala523=
NM_000313.3:c.1961C= , LRG_572t1:c.1961C= NP_000304.2:p.Ala654=
NM_001314077.1:c.2057C= , LRG_572t2:c.2057C= NP_001301006.1:p.Ala686=
NM_000313.4:c.1961C= MANE Select NP_000304.2:p.Ala654=
NM_001314077.2:c.2057C= NP_001301006.1:p.Ala686=