Canonical Allele Identifier: CA78477854
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs199469498
MyVariant Identifiers: chr3:g.93603574_93603578del (hg19) chr3:g.93884730_93884734del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93884732_93884736del , CM000665.2:g.93884732_93884736del GRCh38
NC_000003.11:g.93603576_93603580del , CM000665.1:g.93603576_93603580del GRCh37
NC_000003.10:g.95086266_95086270del NCBI36
NG_009813.1:g.94357_94361del , LRG_572:g.94357_94361del

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1486_1490del ENSP00000330021.7:p.Asp496Ter
ENST00000394236.9:c.1486_1490del MANE Select ENSP00000377783.3:p.Asp496Ter
ENST00000407433.6:c.1441_1445del ENSP00000385794.2:p.Asp481Ter
ENST00000647936.1:c.1486_1490del ENSP00000496822.1:p.Asp496Ter
ENST00000648381.1:n.1654_1658del
ENST00000648853.1:c.1444_1448del ENSP00000497262.1:p.Asp482Ter
ENST00000649103.1:c.1585_1589del ENSP00000497962.1:n.1585_1589del
ENST00000649585.1:c.241_245del ENSP00000498163.1:p.Asp81Ter
ENST00000650591.1:c.1582_1586del ENSP00000497376.1:p.Asp528Ter
ENST00000394236.7:c.1486_1490del ENSP00000377783.3:p.Asp496Ter
ENST00000407433.5:c.1093_1097del ENSP00000385794.1:p.Asp365Ter
NM_000313.3:c.1486_1490del , LRG_572t1:c.1486_1490del NP_000304.2:p.Asp496Ter
NM_001314077.1:c.1582_1586del , LRG_572t2:c.1582_1586del NP_001301006.1:p.Asp528Ter
NM_000313.4:c.1486_1490del MANE Select NP_000304.2:p.Asp496Ter
NM_001314077.2:c.1582_1586del NP_001301006.1:p.Asp528Ter
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