Canonical Allele Identifier: CA830349965

Gene: FBXL4

Linked Data

• dbSNP Id: rs1311039275
• MyVariant Identifiers: chr6:g.99323823_99323824insAGACAGAAGATGTTAATGAATTA (hg19) ; chr6:g.98875947_98875948insAGACAGAAGATGTTAATGAATTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875949_98875971dup , CM000668.2:g.98875949_98875971dup	GRCh38
NC_000006.11:g.99323825_99323847dup , CM000668.1:g.99323825_99323847dup	GRCh37
NC_000006.10:g.99430546_99430568dup	NCBI36
NG_033903.1:g.77037_77059dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1390-243_1390-221dup MANE Select	ENSP00000358247.1:n.1390-243_1390-221dup
ENST00000229971.2:c.1390-243_1390-221dup	ENSP00000229971.1:n.1390-243_1390-221dup
ENST00000369244.6:c.1390-243_1390-221dup	ENSP00000358247.1:n.1390-243_1390-221dup
NM_001278716.1:c.1390-243_1390-221dup	NP_001265645.1:n.1390-243_1390-221dup
NM_012160.4:c.1390-243_1390-221dup	NP_036292.2:n.1390-243_1390-221dup
NR_103836.1:n.1435-243_1435-221dup
XM_005266930.1:c.1318-243_1318-221dup	XP_005266987.1:n.1318-243_1318-221dup
XM_005266930.3:c.1318-243_1318-221dup	XP_005266987.1:n.1318-243_1318-221dup
XM_017010726.1:c.1390-243_1390-221dup	XP_016866215.1:n.1390-243_1390-221dup
XM_017010727.2:c.1318-243_1318-221dup	XP_016866216.1:n.1318-243_1318-221dup
XM_017010728.1:c.664-243_664-221dup	XP_016866217.1:n.664-243_664-221dup
NM_001278716.2:c.1390-243_1390-221dup MANE Select	NP_001265645.1:n.1390-243_1390-221dup
NR_103836.2:n.1375-243_1375-221dup
NM_012160.5:c.1390-243_1390-221dup	NP_036292.2:n.1390-243_1390-221dup