Canonical Allele Identifier: CA1649862305

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875098_98875100delinsTTC , CM000668.2:g.98875098_98875100delinsTTC	GRCh38
NC_000006.11:g.99322974_99322976delinsTTC , CM000668.1:g.99322974_99322976delinsTTC	GRCh37
NC_000006.10:g.99429695_99429697delinsTTC	NCBI36
NG_033903.1:g.77907_77909delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+315_1702+317delinsGAA MANE Select	ENSP00000358247.1:n.1702+315_1702+317delinsGAA
ENST00000229971.2:c.1702+315_1702+317delinsGAA	ENSP00000229971.1:n.1702+315_1702+317delinsGAA
ENST00000369244.6:c.1702+315_1702+317delinsGAA	ENSP00000358247.1:n.1702+315_1702+317delinsGAA
NM_001278716.1:c.1702+315_1702+317delinsGAA	NP_001265645.1:n.1702+315_1702+317delinsGAA
NM_012160.4:c.1702+315_1702+317delinsGAA	NP_036292.2:n.1702+315_1702+317delinsGAA
NR_103836.1:n.1747+315_1747+317delinsGAA
XM_005266930.1:c.1630+315_1630+317delinsGAA	XP_005266987.1:n.1630+315_1630+317delinsGAA
XM_005266930.3:c.1630+315_1630+317delinsGAA	XP_005266987.1:n.1630+315_1630+317delinsGAA
XM_017010726.1:c.1702+315_1702+317delinsGAA	XP_016866215.1:n.1702+315_1702+317delinsGAA
XM_017010727.2:c.1630+315_1630+317delinsGAA	XP_016866216.1:n.1630+315_1630+317delinsGAA
XM_017010728.1:c.976+315_976+317delinsGAA	XP_016866217.1:n.976+315_976+317delinsGAA
NM_001278716.2:c.1702+315_1702+317delinsGAA MANE Select	NP_001265645.1:n.1702+315_1702+317delinsGAA
NR_103836.2:n.1687+315_1687+317delinsGAA
NM_012160.5:c.1702+315_1702+317delinsGAA	NP_036292.2:n.1702+315_1702+317delinsGAA