Canonical Allele Identifier: CA1649862505
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875269_98875294delinsTGCATTTCCTATCAAACCAAGCCATC , CM000668.2:g.98875269_98875294delinsTGCATTTCCTATCAAACCAAGCCATC GRCh38
NC_000006.11:g.99323145_99323170delinsTGCATTTCCTATCAAACCAAGCCATC , CM000668.1:g.99323145_99323170delinsTGCATTTCCTATCAAACCAAGCCATC GRCh37
NC_000006.10:g.99429866_99429891delinsTGCATTTCCTATCAAACCAAGCCATC NCBI36
NG_033903.1:g.77713_77738delinsGATGGCTTGGTTTGATAGGAAATGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA MANE Select ENSP00000358247.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAG...
ENST00000229971.2:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA ENSP00000229971.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAG...
ENST00000369244.6:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA ENSP00000358247.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAG...
NM_001278716.1:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA NP_001265645.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAA...
NM_012160.4:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA NP_036292.2:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATG...
NR_103836.1:n.1747+121_1747+146delinsGATGGCTTGGTTTGATAGGAAATGCA
XM_005266930.1:c.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAAATGCA XP_005266987.1:n.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAA...
XM_005266930.3:c.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAAATGCA XP_005266987.1:n.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAA...
XM_017010726.1:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA XP_016866215.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAA...
XM_017010727.2:c.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAAATGCA XP_016866216.1:n.1630+121_1630+146delinsGATGGCTTGGTTTGATAGGAA...
XM_017010728.1:c.976+121_976+146delinsGATGGCTTGGTTTGATAGGAAATGCA XP_016866217.1:n.976+121_976+146delinsGATGGCTTGGTTTGATAGGAAAT...
NM_001278716.2:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA MANE Select NP_001265645.1:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAA...
NR_103836.2:n.1687+121_1687+146delinsGATGGCTTGGTTTGATAGGAAATGCA
NM_012160.5:c.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATGCA NP_036292.2:n.1702+121_1702+146delinsGATGGCTTGGTTTGATAGGAAATG...