Canonical Allele Identifier: CA353671667
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93879176G>T , CM000665.2:g.93879176G>T GRCh38
NC_000003.11:g.93598020G>T , CM000665.1:g.93598020G>T GRCh37
NC_000003.10:g.95080710G>T NCBI36
NG_009813.1:g.99915C>A , LRG_572:g.99915C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1631C>A ENSP00000330021.7:p.Ser544Tyr
ENST00000394236.9:c.1631C>A MANE Select ENSP00000377783.3:p.Ser544Tyr
ENST00000407433.6:c.1586C>A ENSP00000385794.2:p.Ser529Tyr
ENST00000647936.1:c.1631C>A ENSP00000496822.1:p.Ser544Tyr
ENST00000648381.1:n.1799C>A
ENST00000648853.1:c.1589C>A ENSP00000497262.1:p.Ser530Tyr
ENST00000649103.1:c.1730C>A ENSP00000497962.1:n.1730C>A
ENST00000649585.1:c.574C>A ENSP00000498163.1:n.574C>A
ENST00000650591.1:c.1727C>A ENSP00000497376.1:p.Ser576Tyr
ENST00000394236.7:c.1631C>A ENSP00000377783.3:p.Ser544Tyr
ENST00000407433.5:c.1238C>A ENSP00000385794.1:p.Ser413Tyr
NM_000313.3:c.1631C>A , LRG_572t1:c.1631C>A NP_000304.2:p.Ser544Tyr
NM_001314077.1:c.1727C>A , LRG_572t2:c.1727C>A NP_001301006.1:p.Ser576Tyr
NM_000313.4:c.1631C>A MANE Select NP_000304.2:p.Ser544Tyr
NM_001314077.2:c.1727C>A NP_001301006.1:p.Ser576Tyr