Canonical Allele Identifier: CA1649863751

Gene: FBXL4

Linked Data

• dbSNP Id: rs1770649639

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875996_98875997del , CM000668.2:g.98875996_98875997del	GRCh38
NC_000006.11:g.99323872_99323873del , CM000668.1:g.99323872_99323873del	GRCh37
NC_000006.10:g.99430593_99430594del	NCBI36
NG_033903.1:g.77010_77011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1390-270_1390-269del MANE Select	ENSP00000358247.1:n.1390-270_1390-269del
ENST00000229971.2:c.1390-270_1390-269del	ENSP00000229971.1:n.1390-270_1390-269del
ENST00000369244.6:c.1390-270_1390-269del	ENSP00000358247.1:n.1390-270_1390-269del
NM_001278716.1:c.1390-270_1390-269del	NP_001265645.1:n.1390-270_1390-269del
NM_012160.4:c.1390-270_1390-269del	NP_036292.2:n.1390-270_1390-269del
NR_103836.1:n.1435-270_1435-269del
XM_005266930.1:c.1318-270_1318-269del	XP_005266987.1:n.1318-270_1318-269del
XM_005266930.3:c.1318-270_1318-269del	XP_005266987.1:n.1318-270_1318-269del
XM_017010726.1:c.1390-270_1390-269del	XP_016866215.1:n.1390-270_1390-269del
XM_017010727.2:c.1318-270_1318-269del	XP_016866216.1:n.1318-270_1318-269del
XM_017010728.1:c.664-270_664-269del	XP_016866217.1:n.664-270_664-269del
NM_001278716.2:c.1390-270_1390-269del MANE Select	NP_001265645.1:n.1390-270_1390-269del
NR_103836.2:n.1375-270_1375-269del
NM_012160.5:c.1390-270_1390-269del	NP_036292.2:n.1390-270_1390-269del