Canonical Allele Identifier: CA2841394529
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537169_139537170insTAA , CM000685.2:g.139537169_139537170insTAA GRCh38
NC_000023.10:g.138619328_138619329insTAA , CM000685.1:g.138619328_138619329insTAA GRCh37
NC_000023.9:g.138446994_138446995insTAA NCBI36
NG_007994.1:g.11434_11435insTAA , LRG_556:g.11434_11435insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.248_249insTAA MANE Select ENSP00000218099.2:p.Arg83delinsSerLys
ENST00000218099.6:c.248_249insTAA ENSP00000218099.2:p.Arg83delinsSerLys
ENST00000394090.2:c.248_249insTAA ENSP00000377650.2:p.Arg83delinsSerLys
ENST00000479617.2:n.241+14_241+15insTAA
NM_000133.3:c.248_249insTAA , LRG_556t1:c.248_249insTAA NP_000124.1:p.Arg83delinsSerLys
NM_001313913.1:c.248_249insTAA NP_001300842.1:p.Arg83delinsSerLys
XM_005262397.3:c.248_249insTAA XP_005262454.1:p.Arg83delinsSerLys
XM_005262397.4:c.248_249insTAA XP_005262454.1:p.Arg83delinsSerLys
NM_000133.4:c.248_249insTAA MANE Select NP_000124.1:p.Arg83delinsSerLys
NM_001313913.2:c.248_249insTAA NP_001300842.1:p.Arg83delinsSerLys