Canonical Allele Identifier: CA1385026897
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874254C= , CM000665.2:g.93874254C= GRCh38
NC_000003.11:g.93593098C= , CM000665.1:g.93593098C= GRCh37
NC_000003.10:g.95075788C= NCBI36
NG_009813.1:g.104837G= , LRG_572:g.104837G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.2022G= ENSP00000330021.7:p.Lys674=
ENST00000394236.9:c.2022G= MANE Select ENSP00000377783.3:p.Lys674=
ENST00000407433.6:c.1977G= ENSP00000385794.2:p.Lys659=
ENST00000647936.1:c.*125G= ENSP00000496822.1:n.*125G=
ENST00000648381.1:n.2190G=
ENST00000648853.1:c.1980G= ENSP00000497262.1:p.Lys660=
ENST00000650591.1:c.2118G= ENSP00000497376.1:p.Lys706=
ENST00000394236.7:c.2022G= ENSP00000377783.3:p.Lys674=
ENST00000407433.5:c.1629G= ENSP00000385794.1:p.Lys543=
NM_000313.3:c.2022G= , LRG_572t1:c.2022G= NP_000304.2:p.Lys674=
NM_001314077.1:c.2118G= , LRG_572t2:c.2118G= NP_001301006.1:p.Lys706=
NM_000313.4:c.2022G= MANE Select NP_000304.2:p.Lys674=
NM_001314077.2:c.2118G= NP_001301006.1:p.Lys706=