Canonical Allele Identifier: CA78505684
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs199469485

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93927331_93927332del , CM000665.2:g.93927331_93927332del GRCh38
NC_000003.11:g.93646175_93646176del , CM000665.1:g.93646175_93646176del GRCh37
NC_000003.10:g.95128865_95128866del NCBI36
NG_009813.1:g.51759_51760del , LRG_572:g.51759_51760del

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.152_153del ENSP00000330021.7:p.Gln51ArgfsTer2
ENST00000394236.9:c.152_153del MANE Select ENSP00000377783.3:p.Gln51ArgfsTer2
ENST00000407433.6:c.152_153del ENSP00000385794.2:p.Gln51ArgfsTer2
ENST00000472684.2:c.-242_-241del ENSP00000419616.2:n.-242_-241del
ENST00000647936.1:c.152_153del ENSP00000496822.1:p.Gln51ArgfsTer2
ENST00000648381.1:n.320_321del
ENST00000648853.1:c.110_111del ENSP00000497262.1:p.Gln37ArgfsTer2
ENST00000649103.1:c.131_132del ENSP00000497962.1:p.Gln44ArgfsTer2
ENST00000650591.1:c.248_249del ENSP00000497376.1:p.Gln83ArgfsTer2
ENST00000348974.4:c.248_249del ENSP00000330021.6:p.Gln83ArgfsTer2
ENST00000394236.7:c.152_153del ENSP00000377783.3:p.Gln51ArgfsTer2
ENST00000407433.5:c.-242_-241del ENSP00000385794.1:n.-242_-241del
ENST00000472684.1:c.-242_-241del ENSP00000419616.1:n.-242_-241del
NM_000313.3:c.152_153del , LRG_572t1:c.152_153del NP_000304.2:p.Gln51ArgfsTer2
NM_001314077.1:c.248_249del , LRG_572t2:c.248_249del NP_001301006.1:p.Gln83ArgfsTer2
NM_000313.4:c.152_153del MANE Select NP_000304.2:p.Gln51ArgfsTer2
NM_001314077.2:c.248_249del NP_001301006.1:p.Gln83ArgfsTer2