Canonical Allele Identifier: CA1385026901
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874265T= , CM000665.2:g.93874265T= GRCh38
NC_000003.11:g.93593109T= , CM000665.1:g.93593109T= GRCh37
NC_000003.10:g.95075799T= NCBI36
NG_009813.1:g.104826A= , LRG_572:g.104826A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.2011A= ENSP00000330021.7:p.Lys671=
ENST00000394236.9:c.2011A= MANE Select ENSP00000377783.3:p.Lys671=
ENST00000407433.6:c.1966A= ENSP00000385794.2:p.Lys656=
ENST00000647936.1:c.*114A= ENSP00000496822.1:n.*114A=
ENST00000648381.1:n.2179A=
ENST00000648853.1:c.1969A= ENSP00000497262.1:p.Lys657=
ENST00000650591.1:c.2107A= ENSP00000497376.1:p.Lys703=
ENST00000394236.7:c.2011A= ENSP00000377783.3:p.Lys671=
ENST00000407433.5:c.1618A= ENSP00000385794.1:p.Lys540=
NM_000313.3:c.2011A= , LRG_572t1:c.2011A= NP_000304.2:p.Lys671=
NM_001314077.1:c.2107A= , LRG_572t2:c.2107A= NP_001301006.1:p.Lys703=
NM_000313.4:c.2011A= MANE Select NP_000304.2:p.Lys671=
NM_001314077.2:c.2107A= NP_001301006.1:p.Lys703=