Canonical Allele Identifier: CA2586972679
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877019dup , CM000665.2:g.93877019dup GRCh38
NC_000003.11:g.93595863dup , CM000665.1:g.93595863dup GRCh37
NC_000003.10:g.95078553dup NCBI36
NG_009813.1:g.102072dup , LRG_572:g.102072dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1817dup ENSP00000330021.7:p.Asp608GlyfsTer?
ENST00000394236.9:c.1817dup MANE Select ENSP00000377783.3:p.Asp608GlyfsTer?
ENST00000407433.6:c.1772dup ENSP00000385794.2:p.Asp593GlyfsTer?
ENST00000647936.1:c.1644+2144dup ENSP00000496822.1:n.1644+2144dup
ENST00000648381.1:n.1985dup
ENST00000648853.1:c.1775dup ENSP00000497262.1:p.Asp594GlyfsTer?
ENST00000649585.1:c.760dup ENSP00000498163.1:n.760dup
ENST00000650591.1:c.1913dup ENSP00000497376.1:p.Asp640GlyfsTer?
ENST00000394236.7:c.1817dup ENSP00000377783.3:p.Asp608GlyfsTer?
ENST00000407433.5:c.1424dup ENSP00000385794.1:p.Asp477GlyfsTer?
NM_000313.3:c.1817dup , LRG_572t1:c.1817dup NP_000304.2:p.Asp608GlyfsTer?
NM_001314077.1:c.1913dup , LRG_572t2:c.1913dup NP_001301006.1:p.Asp640GlyfsTer?
NM_000313.4:c.1817dup MANE Select NP_000304.2:p.Asp608GlyfsTer?
NM_001314077.2:c.1913dup NP_001301006.1:p.Asp640GlyfsTer?