Canonical Allele Identifier: CA1385038335
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896677G= , CM000665.2:g.93896677G= GRCh38
NC_000003.11:g.93615521G= , CM000665.1:g.93615521G= GRCh37
NC_000003.10:g.95098211G= NCBI36
NG_009813.1:g.82414C= , LRG_572:g.82414C=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.864C= ENSP00000330021.7:p.Cys288=
ENST00000394236.9:c.864C= MANE Select ENSP00000377783.3:p.Cys288=
ENST00000407433.6:c.819C= ENSP00000385794.2:p.Cys273=
ENST00000647936.1:c.864C= ENSP00000496822.1:p.Cys288=
ENST00000648381.1:n.1032C=
ENST00000648853.1:c.822C= ENSP00000497262.1:p.Cys274=
ENST00000649103.1:c.963C= ENSP00000497962.1:n.963C=
ENST00000650591.1:c.960C= ENSP00000497376.1:p.Cys320=
ENST00000394236.7:c.864C= ENSP00000377783.3:p.Cys288=
ENST00000407433.5:c.471C= ENSP00000385794.1:p.Cys157=
NM_000313.3:c.864C= , LRG_572t1:c.864C= NP_000304.2:p.Cys288=
NM_001314077.1:c.960C= , LRG_572t2:c.960C= NP_001301006.1:p.Cys320=
NM_000313.4:c.864C= MANE Select NP_000304.2:p.Cys288=
NM_001314077.2:c.960C= NP_001301006.1:p.Cys320=