Canonical Allele Identifier: CA2839194698
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537134_139537135insA , CM000685.2:g.139537134_139537135insA GRCh38
NC_000023.10:g.138619293_138619294insA , CM000685.1:g.138619293_138619294insA GRCh37
NC_000023.9:g.138446959_138446960insA NCBI36
NG_007994.1:g.11399_11400insA , LRG_556:g.11399_11400insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.213_214insA MANE Select ENSP00000218099.2:p.Glu72ArgfsTer8
ENST00000218099.6:c.213_214insA ENSP00000218099.2:p.Glu72ArgfsTer8
ENST00000394090.2:c.213_214insA ENSP00000377650.2:p.Glu72ArgfsTer8
ENST00000479617.2:n.220_221insA
NM_000133.3:c.213_214insA , LRG_556t1:c.213_214insA NP_000124.1:p.Glu72ArgfsTer8
NM_001313913.1:c.213_214insA NP_001300842.1:p.Glu72ArgfsTer8
XM_005262397.3:c.213_214insA XP_005262454.1:p.Glu72ArgfsTer8
XM_005262397.4:c.213_214insA XP_005262454.1:p.Glu72ArgfsTer8
NM_000133.4:c.213_214insA MANE Select NP_000124.1:p.Glu72ArgfsTer8
NM_001313913.2:c.213_214insA NP_001300842.1:p.Glu72ArgfsTer8