Canonical Allele Identifier: CA3933537

Gene: FBXL4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98905402del , CM000668.2:g.98905402del	GRCh38
NC_000006.11:g.99353278del , CM000668.1:g.99353278del	GRCh37
NC_000006.10:g.99459999del	NCBI36
NG_033903.1:g.47611del

Transcript Alleles

HGVS	Amino-acid Change
NM_001278716.2:c.1103+30del MANE Select	NP_001265645.1:n.1103+30del
ENST00000369244.7:c.1103+30del MANE Select	ENSP00000358247.1:n.1103+30del
NM_001278716.1:c.1103+30del	NP_001265645.1:n.1103+30del
NM_012160.4:c.1103+30del	NP_036292.2:n.1103+30del
NM_012160.5:c.1103+30del	NP_036292.2:n.1103+30del
NR_103836.1:n.1148+30del
NR_103836.2:n.1088+30del
NR_103837.1:n.1148+30del
NR_103837.2:n.1088+30del
ENST00000229971.2:c.1103+30del	ENSP00000229971.1:n.1103+30del
ENST00000369244.6:c.1103+30del	ENSP00000358247.1:n.1103+30del
XM_005266930.1:c.1103+30del	XP_005266987.1:n.1103+30del
XM_005266930.3:c.1103+30del	XP_005266987.1:n.1103+30del
XM_011535748.1:c.1103+30del	XP_011534050.1:n.1103+30del
XM_011535748.3:c.1103+30del	XP_011534050.1:n.1103+30del
XM_017010726.1:c.1103+30del	XP_016866215.1:n.1103+30del
XM_017010727.2:c.1103+30del	XP_016866216.1:n.1103+30del
XM_017010728.1:c.377+30del	XP_016866217.1:n.377+30del