Canonical Allele Identifier: CA2666653092
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874103_93874108del , CM000665.2:g.93874103_93874108del GRCh38
NC_000003.11:g.93592947_93592952del , CM000665.1:g.93592947_93592952del GRCh37
NC_000003.10:g.95075637_95075642del NCBI36
NG_009813.1:g.104984_104989del , LRG_572:g.104984_104989del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.*1+137_*1+142del ENSP00000330021.7:n.*1+137_*1+142del
ENST00000394236.9:c.*138_*143del MANE Select ENSP00000377783.3:n.*138_*143del
ENST00000407433.6:c.*138_*143del ENSP00000385794.2:n.*138_*143del
ENST00000647936.1:c.*272_*277del ENSP00000496822.1:n.*272_*277del
ENST00000648381.1:n.2337_2342del
ENST00000648853.1:c.*138_*143del ENSP00000497262.1:n.*138_*143del
ENST00000650591.1:c.*138_*143del ENSP00000497376.1:n.*138_*143del
ENST00000394236.7:c.*138_*143del ENSP00000377783.3:n.*138_*143del
ENST00000407433.5:c.*138_*143del ENSP00000385794.1:n.*138_*143del
NM_000313.3:c.*138_*143del , LRG_572t1:c.*138_*143del NP_000304.2:n.*138_*143del
NM_001314077.1:c.*138_*143del , LRG_572t2:c.*138_*143del NP_001301006.1:n.*138_*143del
NM_000313.4:c.*138_*143del MANE Select NP_000304.2:n.*138_*143del
NM_001314077.2:c.*138_*143del NP_001301006.1:n.*138_*143del