Canonical Allele Identifier: CA1649862311

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875107_98875113delinsTAATAAA , CM000668.2:g.98875107_98875113delinsTAATAAA	GRCh38
NC_000006.11:g.99322983_99322989delinsTAATAAA , CM000668.1:g.99322983_99322989delinsTAATAAA	GRCh37
NC_000006.10:g.99429704_99429710delinsTAATAAA	NCBI36
NG_033903.1:g.77894_77900delinsTTTATTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+302_1702+308delinsTTTATTA MANE Select	ENSP00000358247.1:n.1702+302_1702+308delinsTTTATTA
ENST00000229971.2:c.1702+302_1702+308delinsTTTATTA	ENSP00000229971.1:n.1702+302_1702+308delinsTTTATTA
ENST00000369244.6:c.1702+302_1702+308delinsTTTATTA	ENSP00000358247.1:n.1702+302_1702+308delinsTTTATTA
NM_001278716.1:c.1702+302_1702+308delinsTTTATTA	NP_001265645.1:n.1702+302_1702+308delinsTTTATTA
NM_012160.4:c.1702+302_1702+308delinsTTTATTA	NP_036292.2:n.1702+302_1702+308delinsTTTATTA
NR_103836.1:n.1747+302_1747+308delinsTTTATTA
XM_005266930.1:c.1630+302_1630+308delinsTTTATTA	XP_005266987.1:n.1630+302_1630+308delinsTTTATTA
XM_005266930.3:c.1630+302_1630+308delinsTTTATTA	XP_005266987.1:n.1630+302_1630+308delinsTTTATTA
XM_017010726.1:c.1702+302_1702+308delinsTTTATTA	XP_016866215.1:n.1702+302_1702+308delinsTTTATTA
XM_017010727.2:c.1630+302_1630+308delinsTTTATTA	XP_016866216.1:n.1630+302_1630+308delinsTTTATTA
XM_017010728.1:c.976+302_976+308delinsTTTATTA	XP_016866217.1:n.976+302_976+308delinsTTTATTA
NM_001278716.2:c.1702+302_1702+308delinsTTTATTA MANE Select	NP_001265645.1:n.1702+302_1702+308delinsTTTATTA
NR_103836.2:n.1687+302_1687+308delinsTTTATTA
NM_012160.5:c.1702+302_1702+308delinsTTTATTA	NP_036292.2:n.1702+302_1702+308delinsTTTATTA