Canonical Allele Identifier: CA1385036838
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93893047T= , CM000665.2:g.93893047T= GRCh38
NC_000003.11:g.93611891T= , CM000665.1:g.93611891T= GRCh37
NC_000003.10:g.95094581T= NCBI36
NG_009813.1:g.86044A= , LRG_572:g.86044A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1041A= ENSP00000330021.7:p.Ser347=
ENST00000394236.9:c.1041A= MANE Select ENSP00000377783.3:p.Ser347=
ENST00000407433.6:c.996A= ENSP00000385794.2:p.Ser332=
ENST00000647936.1:c.1041A= ENSP00000496822.1:p.Ser347=
ENST00000648381.1:n.1209A=
ENST00000648853.1:c.999A= ENSP00000497262.1:p.Ser333=
ENST00000649103.1:c.1140A= ENSP00000497962.1:n.1140A=
ENST00000650591.1:c.1137A= ENSP00000497376.1:p.Ser379=
ENST00000394236.7:c.1041A= ENSP00000377783.3:p.Ser347=
ENST00000407433.5:c.648A= ENSP00000385794.1:p.Ser216=
NM_000313.3:c.1041A= , LRG_572t1:c.1041A= NP_000304.2:p.Ser347=
NM_001314077.1:c.1137A= , LRG_572t2:c.1137A= NP_001301006.1:p.Ser379=
NM_000313.4:c.1041A= MANE Select NP_000304.2:p.Ser347=
NM_001314077.2:c.1137A= NP_001301006.1:p.Ser379=