Canonical Allele Identifier: CA1385038295
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93896585T= , CM000665.2:g.93896585T= GRCh38
NC_000003.11:g.93615429T= , CM000665.1:g.93615429T= GRCh37
NC_000003.10:g.95098119T= NCBI36
NG_009813.1:g.82506A= , LRG_572:g.82506A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.956A= ENSP00000330021.7:p.Glu319=
ENST00000394236.9:c.956A= MANE Select ENSP00000377783.3:p.Glu319=
ENST00000407433.6:c.911A= ENSP00000385794.2:p.Glu304=
ENST00000647936.1:c.956A= ENSP00000496822.1:p.Glu319=
ENST00000648381.1:n.1124A=
ENST00000648853.1:c.914A= ENSP00000497262.1:p.Glu305=
ENST00000649103.1:c.1055A= ENSP00000497962.1:n.1055A=
ENST00000650591.1:c.1052A= ENSP00000497376.1:p.Glu351=
ENST00000394236.7:c.956A= ENSP00000377783.3:p.Glu319=
ENST00000407433.5:c.563A= ENSP00000385794.1:p.Glu188=
NM_000313.3:c.956A= , LRG_572t1:c.956A= NP_000304.2:p.Glu319=
NM_001314077.1:c.1052A= , LRG_572t2:c.1052A= NP_001301006.1:p.Glu351=
NM_000313.4:c.956A= MANE Select NP_000304.2:p.Glu319=
NM_001314077.2:c.1052A= NP_001301006.1:p.Glu351=