Canonical Allele Identifier: CA2740769618

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98927014_98927015insG , CM000668.2:g.98927014_98927015insG	GRCh38
NC_000006.11:g.99374890_99374891insG , CM000668.1:g.99374890_99374891insG	GRCh37
NC_000006.10:g.99481611_99481612insG	NCBI36
NG_033903.1:g.25992_25993insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.-27_-26insC MANE Select	ENSP00000358247.1:n.-27_-26insC
ENST00000229971.2:c.-27_-26insC	ENSP00000229971.1:n.-27_-26insC
ENST00000369244.6:c.-27_-26insC	ENSP00000358247.1:n.-27_-26insC
NM_001278716.1:c.-27_-26insC	NP_001265645.1:n.-27_-26insC
NM_012160.4:c.-27_-26insC	NP_036292.2:n.-27_-26insC
NR_103836.1:n.365_366insC
NR_103837.1:n.365_366insC
XM_005266930.1:c.-27_-26insC	XP_005266987.1:n.-27_-26insC
XM_011535748.1:c.-27_-26insC	XP_011534050.1:n.-27_-26insC
XM_005266930.3:c.-27_-26insC	XP_005266987.1:n.-27_-26insC
XM_011535748.3:c.-27_-26insC	XP_011534050.1:n.-27_-26insC
XM_017010726.1:c.-27_-26insC	XP_016866215.1:n.-27_-26insC
XM_017010727.2:c.-27_-26insC	XP_016866216.1:n.-27_-26insC
XM_017010728.1:c.-829_-828insC	XP_016866217.1:n.-829_-828insC
NM_001278716.2:c.-27_-26insC MANE Select	NP_001265645.1:n.-27_-26insC
NR_103836.2:n.305_306insC
NR_103837.2:n.305_306insC
NM_012160.5:c.-27_-26insC	NP_036292.2:n.-27_-26insC