Canonical Allele Identifier: CA2545901081
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93898365del , CM000665.2:g.93898365del GRCh38
NC_000003.11:g.93617209del , CM000665.1:g.93617209del GRCh37
NC_000003.10:g.95099899del NCBI36
NG_009813.1:g.80727del , LRG_572:g.80727del

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.849+84del ENSP00000330021.7:n.849+84del
ENST00000394236.9:c.849+84del MANE Select ENSP00000377783.3:n.849+84del
ENST00000407433.6:c.804+84del ENSP00000385794.2:n.804+84del
ENST00000647936.1:c.849+84del ENSP00000496822.1:n.849+84del
ENST00000648381.1:n.1017+84del
ENST00000648853.1:c.807+84del ENSP00000497262.1:n.807+84del
ENST00000649103.1:c.948+84del ENSP00000497962.1:n.948+84del
ENST00000650591.1:c.945+84del ENSP00000497376.1:n.945+84del
ENST00000394236.7:c.849+84del ENSP00000377783.3:n.849+84del
ENST00000407433.5:c.456+84del ENSP00000385794.1:n.456+84del
NM_000313.3:c.849+84del , LRG_572t1:c.849+84del NP_000304.2:n.849+84del
NM_001314077.1:c.945+84del , LRG_572t2:c.945+84del NP_001301006.1:n.945+84del
NM_000313.4:c.849+84del MANE Select NP_000304.2:n.849+84del
NM_001314077.2:c.945+84del NP_001301006.1:n.945+84del