Canonical Allele Identifier: CA912683017
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1328875530

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93873828del , CM000665.2:g.93873828del GRCh38
NC_000003.11:g.93592672del , CM000665.1:g.93592672del GRCh37
NC_000003.10:g.95075362del NCBI36
NG_009813.1:g.105267del , LRG_572:g.105267del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.*2-411del ENSP00000330021.7:n.*2-411del
ENST00000394236.9:c.*421del MANE Select ENSP00000377783.3:n.*421del
ENST00000407433.6:c.*421del ENSP00000385794.2:n.*421del
ENST00000647936.1:c.*555del ENSP00000496822.1:n.*555del
ENST00000648381.1:n.2620del
ENST00000648853.1:c.*421del ENSP00000497262.1:n.*421del
ENST00000650591.1:c.*421del ENSP00000497376.1:n.*421del
ENST00000394236.7:c.*421del ENSP00000377783.3:n.*421del
ENST00000407433.5:c.*421del ENSP00000385794.1:n.*421del
NM_000313.3:c.*421del , LRG_572t1:c.*421del NP_000304.2:n.*421del
NM_001314077.1:c.*421del , LRG_572t2:c.*421del NP_001301006.1:n.*421del
NM_000313.4:c.*421del MANE Select NP_000304.2:n.*421del
NM_001314077.2:c.*421del NP_001301006.1:n.*421del