Canonical Allele Identifier: CA10581427
Gene: FBXL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 235778
dbSNP Id: rs878853112

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98875556_98875573del , CM000668.2:g.98875556_98875573del GRCh38
NC_000006.11:g.99323432_99323449del , CM000668.1:g.99323432_99323449del GRCh37
NC_000006.10:g.99430153_99430170del NCBI36
NG_033903.1:g.77436_77453del

Transcript Alleles

HGVS Amino-acid change
ENST00000369244.7:c.1546_1563del MANE Select ENSP00000358247.1:p.Pro516_Ser521del
ENST00000229971.2:c.1546_1563del ENSP00000229971.1:p.Pro516_Ser521del
ENST00000369244.6:c.1546_1563del ENSP00000358247.1:p.Pro516_Ser521del
NM_001278716.1:c.1546_1563del NP_001265645.1:p.Pro516_Ser521del
NM_012160.4:c.1546_1563del NP_036292.2:p.Pro516_Ser521del
NR_103836.1:n.1591_1608del
XM_005266930.1:c.1474_1491del XP_005266987.1:p.Pro492_Ser497del
XM_005266930.3:c.1474_1491del XP_005266987.1:p.Pro492_Ser497del
XM_017010726.1:c.1546_1563del XP_016866215.1:p.Pro516_Ser521del
XM_017010727.2:c.1474_1491del XP_016866216.1:p.Pro492_Ser497del
XM_017010728.1:c.820_837del XP_016866217.1:p.Pro274_Ser279del
NM_001278716.2:c.1546_1563del MANE Select NP_001265645.1:p.Pro516_Ser521del
NR_103836.2:n.1531_1548del
NM_012160.5:c.1546_1563del NP_036292.2:p.Pro516_Ser521del