Canonical Allele Identifier: CA78490898
Gene: PROS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905802_93905809delinsGCTTTCA , CM000665.2:g.93905802_93905809delinsGCTTTCA GRCh38
NC_000003.11:g.93624646_93624653delinsGCTTTCA , CM000665.1:g.93624646_93624653delinsGCTTTCA GRCh37
NC_000003.10:g.95107336_95107343delinsGCTTTCA NCBI36
NG_009813.1:g.73282_73289delinsTGAAAGC , LRG_572:g.73282_73289delinsTGAAAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.576_583delinsTGAAAGC ENSP00000330021.7:p.Met192IlefsTer16
ENST00000394236.9:c.576_583delinsTGAAAGC MANE Select ENSP00000377783.3:p.Met192IlefsTer16
ENST00000407433.6:c.556+20_556+27delinsTGAAAGC ENSP00000385794.2:n.556+20_556+27delinsTGAAAGC
ENST00000647936.1:c.576_583delinsTGAAAGC ENSP00000496822.1:p.Met192IlefsTer16
ENST00000648381.1:n.744_751delinsTGAAAGC
ENST00000648853.1:c.534_541delinsTGAAAGC ENSP00000497262.1:p.Met178IlefsTer16
ENST00000649103.1:c.675_682delinsTGAAAGC ENSP00000497962.1:n.675_682delinsTGAAAGC
ENST00000650591.1:c.672_679delinsTGAAAGC ENSP00000497376.1:p.Met224IlefsTer16
ENST00000348974.4:c.672_679delinsTGAAAGC ENSP00000330021.6:p.Met224IlefsTer?
ENST00000394236.7:c.576_583delinsTGAAAGC ENSP00000377783.3:p.Met192IlefsTer16
ENST00000407433.5:c.183_190delinsTGAAAGC ENSP00000385794.1:p.Met61IlefsTer16
NM_000313.3:c.576_583delinsTGAAAGC , LRG_572t1:c.576_583delinsTGAAAGC NP_000304.2:p.Met192IlefsTer16
NM_001314077.1:c.672_679delinsTGAAAGC , LRG_572t2:c.672_679delinsTGAAAGC NP_001301006.1:p.Met224IlefsTer16
NM_000313.4:c.576_583delinsTGAAAGC MANE Select NP_000304.2:p.Met192IlefsTer16
NM_001314077.2:c.672_679delinsTGAAAGC NP_001301006.1:p.Met224IlefsTer16
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