Canonical Allele Identifier: CA2823819900
Gene: F9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139548296_139548297insGGAAAGAA , CM000685.2:g.139548296_139548297insGGAAAGAA GRCh38
NC_000023.10:g.138630455_138630456insGGAAAGAA , CM000685.1:g.138630455_138630456insGGAAAGAA GRCh37
NC_000023.9:g.138458121_138458122insGGAAAGAA NCBI36
NG_007994.1:g.22561_22562insGGAAAGAA , LRG_556:g.22561_22562insGGAAAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.392-67_392-66insGGAAAGAA MANE Select ENSP00000218099.2:n.392-67_392-66insGGAAAGAA
ENST00000643157.1:n.1059-67_1059-66insGGAAAGAA
ENST00000218099.6:c.392-67_392-66insGGAAAGAA ENSP00000218099.2:n.392-67_392-66insGGAAAGAA
ENST00000394090.2:c.278-67_278-66insGGAAAGAA ENSP00000377650.2:n.278-67_278-66insGGAAAGAA
ENST00000479617.2:n.345-67_345-66insGGAAAGAA
NM_000133.3:c.392-67_392-66insGGAAAGAA , LRG_556t1:c.392-67_392-66insGGAAAGAA NP_000124.1:n.392-67_392-66insGGAAAGAA
NM_001313913.1:c.278-67_278-66insGGAAAGAA NP_001300842.1:n.278-67_278-66insGGAAAGAA
XM_005262397.3:c.392-2766_392-2765insGGAAAGAA XP_005262454.1:n.392-2766_392-2765insGGAAAGAA
XM_005262397.4:c.392-2766_392-2765insGGAAAGAA XP_005262454.1:n.392-2766_392-2765insGGAAAGAA
NM_000133.4:c.392-67_392-66insGGAAAGAA MANE Select NP_000124.1:n.392-67_392-66insGGAAAGAA
NM_001313913.2:c.278-67_278-66insGGAAAGAA NP_001300842.1:n.278-67_278-66insGGAAAGAA