Canonical Allele Identifier: CA2461412261
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs1928128260

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561945del , CM000685.2:g.139561945del GRCh38
NC_000023.10:g.138644104del , CM000685.1:g.138644104del GRCh37
NC_000023.9:g.138471770del NCBI36
NG_007994.1:g.36210del , LRG_556:g.36210del

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1260del MANE Select ENSP00000218099.2:p.Thr422ProfsTer4
ENST00000643157.1:n.1723+204del
ENST00000218099.6:c.1260del ENSP00000218099.2:p.Thr422ProfsTer4
ENST00000394090.2:c.1146del ENSP00000377650.2:p.Thr384ProfsTer4
NM_000133.3:c.1260del , LRG_556t1:c.1260del NP_000124.1:p.Thr422ProfsTer4
NM_001313913.1:c.1146del NP_001300842.1:p.Thr384ProfsTer4
XM_005262397.3:c.1131del XP_005262454.1:p.Thr379ProfsTer4
XM_005262397.4:c.1131del XP_005262454.1:p.Thr379ProfsTer4
NM_000133.4:c.1260del MANE Select NP_000124.1:p.Thr422ProfsTer4
NM_001313913.2:c.1146del NP_001300842.1:p.Thr384ProfsTer4