Canonical Allele Identifier: CA2679759293
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98926638_98926639insAT , CM000668.2:g.98926638_98926639insAT GRCh38
NC_000006.11:g.99374514_99374515insAT , CM000668.1:g.99374514_99374515insAT GRCh37
NC_000006.10:g.99481235_99481236insAT NCBI36
NG_033903.1:g.26368_26369insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.350_351insAT MANE Select ENSP00000358247.1:p.Pro118CysfsTer27
ENST00000229971.2:c.350_351insAT ENSP00000229971.1:p.Pro118CysfsTer27
ENST00000369244.6:c.350_351insAT ENSP00000358247.1:p.Pro118CysfsTer27
NM_001278716.1:c.350_351insAT NP_001265645.1:p.Pro118CysfsTer27
NM_012160.4:c.350_351insAT NP_036292.2:p.Pro118CysfsTer27
NR_103836.1:n.741_742insAT
NR_103837.1:n.741_742insAT
XM_005266930.1:c.350_351insAT XP_005266987.1:p.Pro118CysfsTer27
XM_011535748.1:c.350_351insAT XP_011534050.1:p.Pro118CysfsTer27
XM_005266930.3:c.350_351insAT XP_005266987.1:p.Pro118CysfsTer27
XM_011535748.3:c.350_351insAT XP_011534050.1:p.Pro118CysfsTer27
XM_017010726.1:c.350_351insAT XP_016866215.1:p.Pro118CysfsTer27
XM_017010727.2:c.350_351insAT XP_016866216.1:p.Pro118CysfsTer27
XM_017010728.1:c.-453_-452insAT XP_016866217.1:n.-453_-452insAT
NM_001278716.2:c.350_351insAT MANE Select NP_001265645.1:p.Pro118CysfsTer27
NR_103836.2:n.681_682insAT
NR_103837.2:n.681_682insAT
NM_012160.5:c.350_351insAT NP_036292.2:p.Pro118CysfsTer27