Canonical Allele Identifier: CA1529373472

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783908_15783909delinsAC , CM000667.2:g.15783908_15783909delinsAC	GRCh38
NC_000005.9:g.15784017_15784018delinsAC , CM000667.1:g.15784017_15784018delinsAC	GRCh37
NC_000005.8:g.15837017_15837018delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-143982_128-143981delinsAC MANE Select	ENSP00000423630.1:n.128-143982_128-143981delinsAC
ENST00000504595.1:c.128-143982_128-143981delinsAC	ENSP00000423630.1:n.128-143982_128-143981delinsAC
ENST00000510662.1:c.-14-143982_-14-143981delinsAC	ENSP00000425184.1:n.-14-143982_-14-143981delinsAC
NM_001278317.1:c.-14-143982_-14-143981delinsAC	NP_001265246.1:n.-14-143982_-14-143981delinsAC
NM_012304.4:c.128-143982_128-143981delinsAC	NP_036436.1:n.128-143982_128-143981delinsAC
XM_005248273.3:c.113-143982_113-143981delinsAC	XP_005248330.1:n.113-143982_113-143981delinsAC
XM_011513998.1:c.-91-50869_-91-50868delinsAC	XP_011512300.1:n.-91-50869_-91-50868delinsAC
XM_017009262.2:c.113-143982_113-143981delinsAC	XP_016864751.1:n.113-143982_113-143981delinsAC
NM_012304.5:c.128-143982_128-143981delinsAC MANE Select	NP_036436.1:n.128-143982_128-143981delinsAC
NM_001278317.2:c.-14-143982_-14-143981delinsAC	NP_001265246.1:n.-14-143982_-14-143981delinsAC