Canonical Allele Identifier: CA1385039138
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93898554G= , CM000665.2:g.93898554G= GRCh38
NC_000003.11:g.93617398G= , CM000665.1:g.93617398G= GRCh37
NC_000003.10:g.95100088G= NCBI36
NG_009813.1:g.80537C= , LRG_572:g.80537C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.743C= ENSP00000330021.7:p.Ser248=
ENST00000394236.9:c.743C= MANE Select ENSP00000377783.3:p.Ser248=
ENST00000407433.6:c.698C= ENSP00000385794.2:p.Ser233=
ENST00000647936.1:c.743C= ENSP00000496822.1:p.Ser248=
ENST00000648381.1:n.911C=
ENST00000648853.1:c.701C= ENSP00000497262.1:p.Ser234=
ENST00000649103.1:c.842C= ENSP00000497962.1:n.842C=
ENST00000650591.1:c.839C= ENSP00000497376.1:p.Ser280=
ENST00000394236.7:c.743C= ENSP00000377783.3:p.Ser248=
ENST00000407433.5:c.350C= ENSP00000385794.1:p.Ser117=
NM_000313.3:c.743C= , LRG_572t1:c.743C= NP_000304.2:p.Ser248=
NM_001314077.1:c.839C= , LRG_572t2:c.839C= NP_001301006.1:p.Ser280=
NM_000313.4:c.743C= MANE Select NP_000304.2:p.Ser248=
NM_001314077.2:c.839C= NP_001301006.1:p.Ser280=