Canonical Allele Identifier: CA1649907135
Gene: FBXL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98926352_98926353delinsGA , CM000668.2:g.98926352_98926353delinsGA GRCh38
NC_000006.11:g.99374228_99374229delinsGA , CM000668.1:g.99374228_99374229delinsGA GRCh37
NC_000006.10:g.99480949_99480950delinsGA NCBI36
NG_033903.1:g.26654_26655delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.512+124_512+125delinsTC MANE Select ENSP00000358247.1:n.512+124_512+125delinsTC
ENST00000229971.2:c.512+124_512+125delinsTC ENSP00000229971.1:n.512+124_512+125delinsTC
ENST00000369244.6:c.512+124_512+125delinsTC ENSP00000358247.1:n.512+124_512+125delinsTC
NM_001278716.1:c.512+124_512+125delinsTC NP_001265645.1:n.512+124_512+125delinsTC
NM_012160.4:c.512+124_512+125delinsTC NP_036292.2:n.512+124_512+125delinsTC
NR_103836.1:n.903+124_903+125delinsTC
NR_103837.1:n.903+124_903+125delinsTC
XM_005266930.1:c.512+124_512+125delinsTC XP_005266987.1:n.512+124_512+125delinsTC
XM_011535748.1:c.512+124_512+125delinsTC XP_011534050.1:n.512+124_512+125delinsTC
XM_005266930.3:c.512+124_512+125delinsTC XP_005266987.1:n.512+124_512+125delinsTC
XM_011535748.3:c.512+124_512+125delinsTC XP_011534050.1:n.512+124_512+125delinsTC
XM_017010726.1:c.512+124_512+125delinsTC XP_016866215.1:n.512+124_512+125delinsTC
XM_017010727.2:c.512+124_512+125delinsTC XP_016866216.1:n.512+124_512+125delinsTC
XM_017010728.1:c.-291+124_-291+125delinsTC XP_016866217.1:n.-291+124_-291+125delinsTC
NM_001278716.2:c.512+124_512+125delinsTC MANE Select NP_001265645.1:n.512+124_512+125delinsTC
NR_103836.2:n.843+124_843+125delinsTC
NR_103837.2:n.843+124_843+125delinsTC
NM_012160.5:c.512+124_512+125delinsTC NP_036292.2:n.512+124_512+125delinsTC