Canonical Allele Identifier: CA451573244
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98926612_98926613del , CM000668.2:g.98926612_98926613del GRCh38
NC_000006.11:g.99374488_99374489del , CM000668.1:g.99374488_99374489del GRCh37
NC_000006.10:g.99481209_99481210del NCBI36
NG_033903.1:g.26395_26396del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.377_378del MANE Select ENSP00000358247.1:p.Tyr126CysfsTer6
ENST00000229971.2:c.377_378del ENSP00000229971.1:p.Tyr126CysfsTer6
ENST00000369244.6:c.377_378del ENSP00000358247.1:p.Tyr126CysfsTer6
NM_001278716.1:c.377_378del NP_001265645.1:p.Tyr126CysfsTer6
NM_012160.4:c.377_378del NP_036292.2:p.Tyr126CysfsTer6
NR_103836.1:n.768_769del
NR_103837.1:n.768_769del
XM_005266930.1:c.377_378del XP_005266987.1:p.Tyr126CysfsTer6
XM_011535748.1:c.377_378del XP_011534050.1:p.Tyr126CysfsTer6
XM_005266930.3:c.377_378del XP_005266987.1:p.Tyr126CysfsTer6
XM_011535748.3:c.377_378del XP_011534050.1:p.Tyr126CysfsTer6
XM_017010726.1:c.377_378del XP_016866215.1:p.Tyr126CysfsTer6
XM_017010727.2:c.377_378del XP_016866216.1:p.Tyr126CysfsTer6
XM_017010728.1:c.-426_-425del XP_016866217.1:n.-426_-425del
NM_001278716.2:c.377_378del MANE Select NP_001265645.1:p.Tyr126CysfsTer6
NR_103836.2:n.708_709del
NR_103837.2:n.708_709del
NM_012160.5:c.377_378del NP_036292.2:p.Tyr126CysfsTer6