Canonical Allele Identifier: CA1649907608

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926699_98926701delinsAAC , CM000668.2:g.98926699_98926701delinsAAC	GRCh38
NC_000006.11:g.99374575_99374577delinsAAC , CM000668.1:g.99374575_99374577delinsAAC	GRCh37
NC_000006.10:g.99481296_99481298delinsAAC	NCBI36
NG_033903.1:g.26306_26308delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.288_290delinsGTT MANE Select	ENSP00000358247.1:p.Val96=
ENST00000229971.2:c.288_290delinsGTT	ENSP00000229971.1:p.Val96=
ENST00000369244.6:c.288_290delinsGTT	ENSP00000358247.1:p.Val96=
NM_001278716.1:c.288_290delinsGTT	NP_001265645.1:p.Val96=
NM_012160.4:c.288_290delinsGTT	NP_036292.2:p.Val96=
NR_103836.1:n.679_681delinsGTT
NR_103837.1:n.679_681delinsGTT
XM_005266930.1:c.288_290delinsGTT	XP_005266987.1:p.Val96=
XM_011535748.1:c.288_290delinsGTT	XP_011534050.1:p.Val96=
XM_005266930.3:c.288_290delinsGTT	XP_005266987.1:p.Val96=
XM_011535748.3:c.288_290delinsGTT	XP_011534050.1:p.Val96=
XM_017010726.1:c.288_290delinsGTT	XP_016866215.1:p.Val96=
XM_017010727.2:c.288_290delinsGTT	XP_016866216.1:p.Val96=
XM_017010728.1:c.-515_-513delinsGTT	XP_016866217.1:n.-515_-513delinsGTT
NM_001278716.2:c.288_290delinsGTT MANE Select	NP_001265645.1:p.Val96=
NR_103836.2:n.619_621delinsGTT
NR_103837.2:n.619_621delinsGTT
NM_012160.5:c.288_290delinsGTT	NP_036292.2:p.Val96=