Canonical Allele Identifier: CA1529373411

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783773_15783774delinsCT , CM000667.2:g.15783773_15783774delinsCT	GRCh38
NC_000005.9:g.15783882_15783883delinsCT , CM000667.1:g.15783882_15783883delinsCT	GRCh37
NC_000005.8:g.15836882_15836883delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144117_128-144116delinsCT MANE Select	ENSP00000423630.1:n.128-144117_128-144116delinsCT
ENST00000504595.1:c.128-144117_128-144116delinsCT	ENSP00000423630.1:n.128-144117_128-144116delinsCT
ENST00000510662.1:c.-14-144117_-14-144116delinsCT	ENSP00000425184.1:n.-14-144117_-14-144116delinsCT
NM_001278317.1:c.-14-144117_-14-144116delinsCT	NP_001265246.1:n.-14-144117_-14-144116delinsCT
NM_012304.4:c.128-144117_128-144116delinsCT	NP_036436.1:n.128-144117_128-144116delinsCT
XM_005248273.3:c.113-144117_113-144116delinsCT	XP_005248330.1:n.113-144117_113-144116delinsCT
XM_011513998.1:c.-91-51004_-91-51003delinsCT	XP_011512300.1:n.-91-51004_-91-51003delinsCT
XM_017009262.2:c.113-144117_113-144116delinsCT	XP_016864751.1:n.113-144117_113-144116delinsCT
NM_012304.5:c.128-144117_128-144116delinsCT MANE Select	NP_036436.1:n.128-144117_128-144116delinsCT
NM_001278317.2:c.-14-144117_-14-144116delinsCT	NP_001265246.1:n.-14-144117_-14-144116delinsCT