Canonical Allele Identifier: CA2808354317
Gene: FBXO39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6780642_6780643insACAACCCAAACACACCCAACA , CM000679.2:g.6780642_6780643insACAACCCAAACACACCCAACA GRCh38
NC_000017.10:g.6683961_6683962insACAACCCAAACACACCCAACA , CM000679.1:g.6683961_6683962insACAACCCAAACACACCCAACA GRCh37
NC_000017.9:g.6624685_6624686insACAACCCAAACACACCCAACA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000321535.5:c.774_775insACAACCCAAACACACCCAACA MANE Select ENSP00000321386.4:p.Cys258_His259insThrThrGlnThrHisProThr
ENST00000321535.4:c.774_775insACAACCCAAACACACCCAACA ENSP00000321386.4:p.Cys258_His259insThrThrGlnThrHisProThr
NM_153230.2:c.774_775insACAACCCAAACACACCCAACA NP_694962.1:p.Cys258_His259insThrThrGlnThrHisProThr
XM_011523697.1:c.774_775insACAACCCAAACACACCCAACA XP_011521999.1:p.Cys258_His259insThrThrGlnThrHisProThr
XR_243544.3:n.952_953insACAACCCAAACACACCCAACA
NM_153230.3:c.774_775insACAACCCAAACACACCCAACA MANE Select NP_694962.1:p.Cys258_His259insThrThrGlnThrHisProThr