Canonical Allele Identifier: CA1649862300

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875094_98875097delinsTTTC , CM000668.2:g.98875094_98875097delinsTTTC	GRCh38
NC_000006.11:g.99322970_99322973delinsTTTC , CM000668.1:g.99322970_99322973delinsTTTC	GRCh37
NC_000006.10:g.99429691_99429694delinsTTTC	NCBI36
NG_033903.1:g.77910_77913delinsGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+318_1702+321delinsGAAA MANE Select	ENSP00000358247.1:n.1702+318_1702+321delinsGAAA
ENST00000229971.2:c.1702+318_1702+321delinsGAAA	ENSP00000229971.1:n.1702+318_1702+321delinsGAAA
ENST00000369244.6:c.1702+318_1702+321delinsGAAA	ENSP00000358247.1:n.1702+318_1702+321delinsGAAA
NM_001278716.1:c.1702+318_1702+321delinsGAAA	NP_001265645.1:n.1702+318_1702+321delinsGAAA
NM_012160.4:c.1702+318_1702+321delinsGAAA	NP_036292.2:n.1702+318_1702+321delinsGAAA
NR_103836.1:n.1747+318_1747+321delinsGAAA
XM_005266930.1:c.1630+318_1630+321delinsGAAA	XP_005266987.1:n.1630+318_1630+321delinsGAAA
XM_005266930.3:c.1630+318_1630+321delinsGAAA	XP_005266987.1:n.1630+318_1630+321delinsGAAA
XM_017010726.1:c.1702+318_1702+321delinsGAAA	XP_016866215.1:n.1702+318_1702+321delinsGAAA
XM_017010727.2:c.1630+318_1630+321delinsGAAA	XP_016866216.1:n.1630+318_1630+321delinsGAAA
XM_017010728.1:c.976+318_976+321delinsGAAA	XP_016866217.1:n.976+318_976+321delinsGAAA
NM_001278716.2:c.1702+318_1702+321delinsGAAA MANE Select	NP_001265645.1:n.1702+318_1702+321delinsGAAA
NR_103836.2:n.1687+318_1687+321delinsGAAA
NM_012160.5:c.1702+318_1702+321delinsGAAA	NP_036292.2:n.1702+318_1702+321delinsGAAA