Canonical Allele Identifier: CA1529373485

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783928_15783929delinsGC , CM000667.2:g.15783928_15783929delinsGC	GRCh38
NC_000005.9:g.15784037_15784038delinsGC , CM000667.1:g.15784037_15784038delinsGC	GRCh37
NC_000005.8:g.15837037_15837038delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-143962_128-143961delinsGC MANE Select	ENSP00000423630.1:n.128-143962_128-143961delinsGC
ENST00000504595.1:c.128-143962_128-143961delinsGC	ENSP00000423630.1:n.128-143962_128-143961delinsGC
ENST00000510662.1:c.-14-143962_-14-143961delinsGC	ENSP00000425184.1:n.-14-143962_-14-143961delinsGC
NM_001278317.1:c.-14-143962_-14-143961delinsGC	NP_001265246.1:n.-14-143962_-14-143961delinsGC
NM_012304.4:c.128-143962_128-143961delinsGC	NP_036436.1:n.128-143962_128-143961delinsGC
XM_005248273.3:c.113-143962_113-143961delinsGC	XP_005248330.1:n.113-143962_113-143961delinsGC
XM_011513998.1:c.-91-50849_-91-50848delinsGC	XP_011512300.1:n.-91-50849_-91-50848delinsGC
XM_017009262.2:c.113-143962_113-143961delinsGC	XP_016864751.1:n.113-143962_113-143961delinsGC
NM_012304.5:c.128-143962_128-143961delinsGC MANE Select	NP_036436.1:n.128-143962_128-143961delinsGC
NM_001278317.2:c.-14-143962_-14-143961delinsGC	NP_001265246.1:n.-14-143962_-14-143961delinsGC