Canonical Allele Identifier: CA1649863680
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875924_98875926delinsTAA , CM000668.2:g.98875924_98875926delinsTAA GRCh38
NC_000006.11:g.99323800_99323802delinsTAA , CM000668.1:g.99323800_99323802delinsTAA GRCh37
NC_000006.10:g.99430521_99430523delinsTAA NCBI36
NG_033903.1:g.77081_77083delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1390-199_1390-197delinsTTA MANE Select ENSP00000358247.1:n.1390-199_1390-197delinsTTA
ENST00000229971.2:c.1390-199_1390-197delinsTTA ENSP00000229971.1:n.1390-199_1390-197delinsTTA
ENST00000369244.6:c.1390-199_1390-197delinsTTA ENSP00000358247.1:n.1390-199_1390-197delinsTTA
NM_001278716.1:c.1390-199_1390-197delinsTTA NP_001265645.1:n.1390-199_1390-197delinsTTA
NM_012160.4:c.1390-199_1390-197delinsTTA NP_036292.2:n.1390-199_1390-197delinsTTA
NR_103836.1:n.1435-199_1435-197delinsTTA
XM_005266930.1:c.1318-199_1318-197delinsTTA XP_005266987.1:n.1318-199_1318-197delinsTTA
XM_005266930.3:c.1318-199_1318-197delinsTTA XP_005266987.1:n.1318-199_1318-197delinsTTA
XM_017010726.1:c.1390-199_1390-197delinsTTA XP_016866215.1:n.1390-199_1390-197delinsTTA
XM_017010727.2:c.1318-199_1318-197delinsTTA XP_016866216.1:n.1318-199_1318-197delinsTTA
XM_017010728.1:c.664-199_664-197delinsTTA XP_016866217.1:n.664-199_664-197delinsTTA
NM_001278716.2:c.1390-199_1390-197delinsTTA MANE Select NP_001265645.1:n.1390-199_1390-197delinsTTA
NR_103836.2:n.1375-199_1375-197delinsTTA
NM_012160.5:c.1390-199_1390-197delinsTTA NP_036292.2:n.1390-199_1390-197delinsTTA