Canonical Allele Identifier: CA1649862494

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875258_98875259delinsCT , CM000668.2:g.98875258_98875259delinsCT	GRCh38
NC_000006.11:g.99323134_99323135delinsCT , CM000668.1:g.99323134_99323135delinsCT	GRCh37
NC_000006.10:g.99429855_99429856delinsCT	NCBI36
NG_033903.1:g.77748_77749delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+156_1702+157delinsAG MANE Select	ENSP00000358247.1:n.1702+156_1702+157delinsAG
ENST00000229971.2:c.1702+156_1702+157delinsAG	ENSP00000229971.1:n.1702+156_1702+157delinsAG
ENST00000369244.6:c.1702+156_1702+157delinsAG	ENSP00000358247.1:n.1702+156_1702+157delinsAG
NM_001278716.1:c.1702+156_1702+157delinsAG	NP_001265645.1:n.1702+156_1702+157delinsAG
NM_012160.4:c.1702+156_1702+157delinsAG	NP_036292.2:n.1702+156_1702+157delinsAG
NR_103836.1:n.1747+156_1747+157delinsAG
XM_005266930.1:c.1630+156_1630+157delinsAG	XP_005266987.1:n.1630+156_1630+157delinsAG
XM_005266930.3:c.1630+156_1630+157delinsAG	XP_005266987.1:n.1630+156_1630+157delinsAG
XM_017010726.1:c.1702+156_1702+157delinsAG	XP_016866215.1:n.1702+156_1702+157delinsAG
XM_017010727.2:c.1630+156_1630+157delinsAG	XP_016866216.1:n.1630+156_1630+157delinsAG
XM_017010728.1:c.976+156_976+157delinsAG	XP_016866217.1:n.976+156_976+157delinsAG
NM_001278716.2:c.1702+156_1702+157delinsAG MANE Select	NP_001265645.1:n.1702+156_1702+157delinsAG
NR_103836.2:n.1687+156_1687+157delinsAG
NM_012160.5:c.1702+156_1702+157delinsAG	NP_036292.2:n.1702+156_1702+157delinsAG