Canonical Allele Identifier: CA2679759292

Gene: FBXL4

Linked Data

• gnomAD v4: 6-98926634-G-GACT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.98926634_98926635insACT , CM000668.2:g.98926634_98926635insACT	GRCh38
NC_000006.11:g.99374510_99374511insACT , CM000668.1:g.99374510_99374511insACT	GRCh37
NC_000006.10:g.99481231_99481232insACT	NCBI36
NG_033903.1:g.26372_26373insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369244.7:c.354_355insAGT MANE Select	ENSP00000358247.1:p.Pro118_Pro119insSer
ENST00000229971.2:c.354_355insAGT	ENSP00000229971.1:p.Pro118_Pro119insSer
ENST00000369244.6:c.354_355insAGT	ENSP00000358247.1:p.Pro118_Pro119insSer
NM_001278716.1:c.354_355insAGT	NP_001265645.1:p.Pro118_Pro119insSer
NM_012160.4:c.354_355insAGT	NP_036292.2:p.Pro118_Pro119insSer
NR_103836.1:n.745_746insAGT
NR_103837.1:n.745_746insAGT
XM_005266930.1:c.354_355insAGT	XP_005266987.1:p.Pro118_Pro119insSer
XM_011535748.1:c.354_355insAGT	XP_011534050.1:p.Pro118_Pro119insSer
XM_005266930.3:c.354_355insAGT	XP_005266987.1:p.Pro118_Pro119insSer
XM_011535748.3:c.354_355insAGT	XP_011534050.1:p.Pro118_Pro119insSer
XM_017010726.1:c.354_355insAGT	XP_016866215.1:p.Pro118_Pro119insSer
XM_017010727.2:c.354_355insAGT	XP_016866216.1:p.Pro118_Pro119insSer
XM_017010728.1:c.-449_-448insAGT	XP_016866217.1:n.-449_-448insAGT
NM_001278716.2:c.354_355insAGT MANE Select	NP_001265645.1:p.Pro118_Pro119insSer
NR_103836.2:n.685_686insAGT
NR_103837.2:n.685_686insAGT
NM_012160.5:c.354_355insAGT	NP_036292.2:p.Pro118_Pro119insSer