Canonical Allele Identifier: CA645546935
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874390_98874391del , CM000668.2:g.98874390_98874391del GRCh38
NC_000006.11:g.99322266_99322267del , CM000668.1:g.99322266_99322267del GRCh37
NC_000006.10:g.99428987_99428988del NCBI36
NG_033903.1:g.78617_78618del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1754_1755del MANE Select ENSP00000358247.1:p.Lys585ArgfsTer6
ENST00000229971.2:c.1754_1755del ENSP00000229971.1:p.Lys585ArgfsTer6
ENST00000369244.6:c.1754_1755del ENSP00000358247.1:p.Lys585ArgfsTer6
NM_001278716.1:c.1754_1755del NP_001265645.1:p.Lys585ArgfsTer6
NM_012160.4:c.1754_1755del NP_036292.2:p.Lys585ArgfsTer6
NR_103836.1:n.1799_1800del
XM_005266930.1:c.1682_1683del XP_005266987.1:p.Lys561ArgfsTer6
XM_005266930.3:c.1682_1683del XP_005266987.1:p.Lys561ArgfsTer6
XM_017010726.1:c.1754_1755del XP_016866215.1:p.Lys585ArgfsTer6
XM_017010727.2:c.1682_1683del XP_016866216.1:p.Lys561ArgfsTer6
XM_017010728.1:c.1028_1029del XP_016866217.1:p.Lys343ArgfsTer6
NM_001278716.2:c.1754_1755del MANE Select NP_001265645.1:p.Lys585ArgfsTer6
NR_103836.2:n.1739_1740del
NM_012160.5:c.1754_1755del NP_036292.2:p.Lys585ArgfsTer6