Canonical Allele Identifier: CA114898709

Gene: FBXL7

Linked Data

• dbSNP Id: rs386685789

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783432_15783433delinsATT , CM000667.2:g.15783432_15783433delinsATT	GRCh38
NC_000005.9:g.15783541_15783542delinsATT , CM000667.1:g.15783541_15783542delinsATT	GRCh37
NC_000005.8:g.15836541_15836542delinsATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144458_128-144457delinsATT MANE Select	ENSP00000423630.1:n.128-144458_128-144457delinsATT
ENST00000504595.1:c.128-144458_128-144457delinsATT	ENSP00000423630.1:n.128-144458_128-144457delinsATT
ENST00000510662.1:c.-14-144458_-14-144457delinsATT	ENSP00000425184.1:n.-14-144458_-14-144457delinsATT
NM_001278317.1:c.-14-144458_-14-144457delinsATT	NP_001265246.1:n.-14-144458_-14-144457delinsATT
NM_012304.4:c.128-144458_128-144457delinsATT	NP_036436.1:n.128-144458_128-144457delinsATT
XM_005248273.3:c.113-144458_113-144457delinsATT	XP_005248330.1:n.113-144458_113-144457delinsATT
XM_011513998.1:c.-91-51345_-91-51344delinsATT	XP_011512300.1:n.-91-51345_-91-51344delinsATT
XM_017009262.2:c.113-144458_113-144457delinsATT	XP_016864751.1:n.113-144458_113-144457delinsATT
NM_012304.5:c.128-144458_128-144457delinsATT MANE Select	NP_036436.1:n.128-144458_128-144457delinsATT
NM_001278317.2:c.-14-144458_-14-144457delinsATT	NP_001265246.1:n.-14-144458_-14-144457delinsATT