Canonical Allele Identifier: CA2586972673
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874265dup , CM000665.2:g.93874265dup GRCh38
NC_000003.11:g.93593109dup , CM000665.1:g.93593109dup GRCh37
NC_000003.10:g.95075799dup NCBI36
NG_009813.1:g.104830dup , LRG_572:g.104830dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.2015dup ENSP00000330021.7:p.Thr673AspfsTer21
ENST00000394236.9:c.2015dup MANE Select ENSP00000377783.3:p.Thr673AspfsTer26
ENST00000407433.6:c.1970dup ENSP00000385794.2:p.Thr658AspfsTer26
ENST00000647936.1:c.*118dup ENSP00000496822.1:n.*118dup
ENST00000648381.1:n.2183dup
ENST00000648853.1:c.1973dup ENSP00000497262.1:p.Thr659AspfsTer26
ENST00000650591.1:c.2111dup ENSP00000497376.1:p.Thr705AspfsTer26
ENST00000394236.7:c.2015dup ENSP00000377783.3:p.Thr673AspfsTer26
ENST00000407433.5:c.1622dup ENSP00000385794.1:p.Thr542AspfsTer26
NM_000313.3:c.2015dup , LRG_572t1:c.2015dup NP_000304.2:p.Thr673AspfsTer26
NM_001314077.1:c.2111dup , LRG_572t2:c.2111dup NP_001301006.1:p.Thr705AspfsTer26
NM_000313.4:c.2015dup MANE Select NP_000304.2:p.Thr673AspfsTer26
NM_001314077.2:c.2111dup NP_001301006.1:p.Thr705AspfsTer26