Canonical Allele Identifier: CA1649860942
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874273_98874275delinsTTA , CM000668.2:g.98874273_98874275delinsTTA GRCh38
NC_000006.11:g.99322149_99322151delinsTTA , CM000668.1:g.99322149_99322151delinsTTA GRCh37
NC_000006.10:g.99428870_99428872delinsTTA NCBI36
NG_033903.1:g.78732_78734delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.*3_*5delinsTAA MANE Select ENSP00000358247.1:n.*3_*5delinsTAA
ENST00000229971.2:c.*3_*5delinsTAA ENSP00000229971.1:n.*3_*5delinsTAA
ENST00000369244.6:c.*3_*5delinsTAA ENSP00000358247.1:n.*3_*5delinsTAA
NM_001278716.1:c.*3_*5delinsTAA NP_001265645.1:n.*3_*5delinsTAA
NM_012160.4:c.*3_*5delinsTAA NP_036292.2:n.*3_*5delinsTAA
NR_103836.1:n.1914_1916delinsTAA
XM_005266930.1:c.*3_*5delinsTAA XP_005266987.1:n.*3_*5delinsTAA
XM_005266930.3:c.*3_*5delinsTAA XP_005266987.1:n.*3_*5delinsTAA
XM_017010726.1:c.*3_*5delinsTAA XP_016866215.1:n.*3_*5delinsTAA
XM_017010727.2:c.*3_*5delinsTAA XP_016866216.1:n.*3_*5delinsTAA
XM_017010728.1:c.*3_*5delinsTAA XP_016866217.1:n.*3_*5delinsTAA
NM_001278716.2:c.*3_*5delinsTAA MANE Select NP_001265645.1:n.*3_*5delinsTAA
NR_103836.2:n.1854_1856delinsTAA
NM_012160.5:c.*3_*5delinsTAA NP_036292.2:n.*3_*5delinsTAA