Canonical Allele Identifier: CA1649861529
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874452_98874467delinsGAAACAAAACAAAACA , CM000668.2:g.98874452_98874467delinsGAAACAAAACAAAACA GRCh38
NC_000006.11:g.99322328_99322343delinsGAAACAAAACAAAACA , CM000668.1:g.99322328_99322343delinsGAAACAAAACAAAACA GRCh37
NC_000006.10:g.99429049_99429064delinsGAAACAAAACAAAACA NCBI36
NG_033903.1:g.78540_78555delinsTGTTTTGTTTTGTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC MANE Select ENSP00000358247.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
ENST00000229971.2:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC ENSP00000229971.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
ENST00000369244.6:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC ENSP00000358247.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
NM_001278716.1:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC NP_001265645.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
NM_012160.4:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC NP_036292.2:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
NR_103836.1:n.1748-26_1748-11delinsTGTTTTGTTTTGTTTC
XM_005266930.1:c.1631-26_1631-11delinsTGTTTTGTTTTGTTTC XP_005266987.1:n.1631-26_1631-11delinsTGTTTTGTTTTGTTTC
XM_005266930.3:c.1631-26_1631-11delinsTGTTTTGTTTTGTTTC XP_005266987.1:n.1631-26_1631-11delinsTGTTTTGTTTTGTTTC
XM_017010726.1:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC XP_016866215.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
XM_017010727.2:c.1631-26_1631-11delinsTGTTTTGTTTTGTTTC XP_016866216.1:n.1631-26_1631-11delinsTGTTTTGTTTTGTTTC
XM_017010728.1:c.977-26_977-11delinsTGTTTTGTTTTGTTTC XP_016866217.1:n.977-26_977-11delinsTGTTTTGTTTTGTTTC
NM_001278716.2:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC MANE Select NP_001265645.1:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC
NR_103836.2:n.1688-26_1688-11delinsTGTTTTGTTTTGTTTC
NM_012160.5:c.1703-26_1703-11delinsTGTTTTGTTTTGTTTC NP_036292.2:n.1703-26_1703-11delinsTGTTTTGTTTTGTTTC