Canonical Allele Identifier: CA1529373298

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783563_15783566delinsAAGG , CM000667.2:g.15783563_15783566delinsAAGG	GRCh38
NC_000005.9:g.15783672_15783675delinsAAGG , CM000667.1:g.15783672_15783675delinsAAGG	GRCh37
NC_000005.8:g.15836672_15836675delinsAAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144327_128-144324delinsAAGG MANE Select	ENSP00000423630.1:n.128-144327_128-144324delinsAAGG
ENST00000504595.1:c.128-144327_128-144324delinsAAGG	ENSP00000423630.1:n.128-144327_128-144324delinsAAGG
ENST00000510662.1:c.-14-144327_-14-144324delinsAAGG	ENSP00000425184.1:n.-14-144327_-14-144324delinsAAGG
NM_001278317.1:c.-14-144327_-14-144324delinsAAGG	NP_001265246.1:n.-14-144327_-14-144324delinsAAGG
NM_012304.4:c.128-144327_128-144324delinsAAGG	NP_036436.1:n.128-144327_128-144324delinsAAGG
XM_005248273.3:c.113-144327_113-144324delinsAAGG	XP_005248330.1:n.113-144327_113-144324delinsAAGG
XM_011513998.1:c.-91-51214_-91-51211delinsAAGG	XP_011512300.1:n.-91-51214_-91-51211delinsAAGG
XM_017009262.2:c.113-144327_113-144324delinsAAGG	XP_016864751.1:n.113-144327_113-144324delinsAAGG
NM_012304.5:c.128-144327_128-144324delinsAAGG MANE Select	NP_036436.1:n.128-144327_128-144324delinsAAGG
NM_001278317.2:c.-14-144327_-14-144324delinsAAGG	NP_001265246.1:n.-14-144327_-14-144324delinsAAGG