Canonical Allele Identifier: CA78477894
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs199469499
MyVariant Identifiers: chr3:g.93603626_93603627del (hg19) chr3:g.93884782_93884783del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93884782_93884783del , CM000665.2:g.93884782_93884783del GRCh38
NC_000003.11:g.93603626_93603627del , CM000665.1:g.93603626_93603627del GRCh37
NC_000003.10:g.95086316_95086317del NCBI36
NG_009813.1:g.94308_94309del , LRG_572:g.94308_94309del

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1437_1438del ENSP00000330021.7:p.Lys481GlyfsTer17
ENST00000394236.9:c.1437_1438del MANE Select ENSP00000377783.3:p.Lys481GlyfsTer17
ENST00000407433.6:c.1392_1393del ENSP00000385794.2:p.Lys466GlyfsTer17
ENST00000647936.1:c.1437_1438del ENSP00000496822.1:p.Lys481GlyfsTer17
ENST00000648381.1:n.1605_1606del
ENST00000648853.1:c.1395_1396del ENSP00000497262.1:p.Lys467GlyfsTer17
ENST00000649103.1:c.1536_1537del ENSP00000497962.1:n.1536_1537del
ENST00000649585.1:c.192_193del ENSP00000498163.1:p.Lys66GlyfsTer17
ENST00000650591.1:c.1533_1534del ENSP00000497376.1:p.Lys513GlyfsTer17
ENST00000394236.7:c.1437_1438del ENSP00000377783.3:p.Lys481GlyfsTer17
ENST00000407433.5:c.1044_1045del ENSP00000385794.1:p.Lys350GlyfsTer17
NM_000313.3:c.1437_1438del , LRG_572t1:c.1437_1438del NP_000304.2:p.Lys481GlyfsTer17
NM_001314077.1:c.1533_1534del , LRG_572t2:c.1533_1534del NP_001301006.1:p.Lys513GlyfsTer17
NM_000313.4:c.1437_1438del MANE Select NP_000304.2:p.Lys481GlyfsTer17
NM_001314077.2:c.1533_1534del NP_001301006.1:p.Lys513GlyfsTer17
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