Canonical Allele Identifier: CA1385026784
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93873984_93873986delinsCTG , CM000665.2:g.93873984_93873986delinsCTG GRCh38
NC_000003.11:g.93592828_93592830delinsCTG , CM000665.1:g.93592828_93592830delinsCTG GRCh37
NC_000003.10:g.95075518_95075520delinsCTG NCBI36
NG_009813.1:g.105105_105107delinsCAG , LRG_572:g.105105_105107delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.*1+258_*1+260delinsCAG ENSP00000330021.7:n.*1+258_*1+260delinsCAG
ENST00000394236.9:c.*259_*261delinsCAG MANE Select ENSP00000377783.3:n.*259_*261delinsCAG
ENST00000407433.6:c.*259_*261delinsCAG ENSP00000385794.2:n.*259_*261delinsCAG
ENST00000647936.1:c.*393_*395delinsCAG ENSP00000496822.1:n.*393_*395delinsCAG
ENST00000648381.1:n.2458_2460delinsCAG
ENST00000648853.1:c.*259_*261delinsCAG ENSP00000497262.1:n.*259_*261delinsCAG
ENST00000650591.1:c.*259_*261delinsCAG ENSP00000497376.1:n.*259_*261delinsCAG
ENST00000394236.7:c.*259_*261delinsCAG ENSP00000377783.3:n.*259_*261delinsCAG
ENST00000407433.5:c.*259_*261delinsCAG ENSP00000385794.1:n.*259_*261delinsCAG
NM_000313.3:c.*259_*261delinsCAG , LRG_572t1:c.*259_*261delinsCAG NP_000304.2:n.*259_*261delinsCAG
NM_001314077.1:c.*259_*261delinsCAG , LRG_572t2:c.*259_*261delinsCAG NP_001301006.1:n.*259_*261delinsCAG
NM_000313.4:c.*259_*261delinsCAG MANE Select NP_000304.2:n.*259_*261delinsCAG
NM_001314077.2:c.*259_*261delinsCAG NP_001301006.1:n.*259_*261delinsCAG