Canonical Allele Identifier: CA1649862271

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98875062_98875063delinsAC , CM000668.2:g.98875062_98875063delinsAC	GRCh38
NC_000006.11:g.99322938_99322939delinsAC , CM000668.1:g.99322938_99322939delinsAC	GRCh37
NC_000006.10:g.99429659_99429660delinsAC	NCBI36
NG_033903.1:g.77944_77945delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.1702+352_1702+353delinsGT MANE Select	ENSP00000358247.1:n.1702+352_1702+353delinsGT
ENST00000229971.2:c.1702+352_1702+353delinsGT	ENSP00000229971.1:n.1702+352_1702+353delinsGT
ENST00000369244.6:c.1702+352_1702+353delinsGT	ENSP00000358247.1:n.1702+352_1702+353delinsGT
NM_001278716.1:c.1702+352_1702+353delinsGT	NP_001265645.1:n.1702+352_1702+353delinsGT
NM_012160.4:c.1702+352_1702+353delinsGT	NP_036292.2:n.1702+352_1702+353delinsGT
NR_103836.1:n.1747+352_1747+353delinsGT
XM_005266930.1:c.1630+352_1630+353delinsGT	XP_005266987.1:n.1630+352_1630+353delinsGT
XM_005266930.3:c.1630+352_1630+353delinsGT	XP_005266987.1:n.1630+352_1630+353delinsGT
XM_017010726.1:c.1702+352_1702+353delinsGT	XP_016866215.1:n.1702+352_1702+353delinsGT
XM_017010727.2:c.1630+352_1630+353delinsGT	XP_016866216.1:n.1630+352_1630+353delinsGT
XM_017010728.1:c.976+352_976+353delinsGT	XP_016866217.1:n.976+352_976+353delinsGT
NM_001278716.2:c.1702+352_1702+353delinsGT MANE Select	NP_001265645.1:n.1702+352_1702+353delinsGT
NR_103836.2:n.1687+352_1687+353delinsGT
NM_012160.5:c.1702+352_1702+353delinsGT	NP_036292.2:n.1702+352_1702+353delinsGT