Canonical Allele Identifier: CA1529373400

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783748_15783752delinsATAGT , CM000667.2:g.15783748_15783752delinsATAGT	GRCh38
NC_000005.9:g.15783857_15783861delinsATAGT , CM000667.1:g.15783857_15783861delinsATAGT	GRCh37
NC_000005.8:g.15836857_15836861delinsATAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144142_128-144138delinsATAGT MANE Select	ENSP00000423630.1:n.128-144142_128-144138delinsATAGT
ENST00000504595.1:c.128-144142_128-144138delinsATAGT	ENSP00000423630.1:n.128-144142_128-144138delinsATAGT
ENST00000510662.1:c.-14-144142_-14-144138delinsATAGT	ENSP00000425184.1:n.-14-144142_-14-144138delinsATAGT
NM_001278317.1:c.-14-144142_-14-144138delinsATAGT	NP_001265246.1:n.-14-144142_-14-144138delinsATAGT
NM_012304.4:c.128-144142_128-144138delinsATAGT	NP_036436.1:n.128-144142_128-144138delinsATAGT
XM_005248273.3:c.113-144142_113-144138delinsATAGT	XP_005248330.1:n.113-144142_113-144138delinsATAGT
XM_011513998.1:c.-91-51029_-91-51025delinsATAGT	XP_011512300.1:n.-91-51029_-91-51025delinsATAGT
XM_017009262.2:c.113-144142_113-144138delinsATAGT	XP_016864751.1:n.113-144142_113-144138delinsATAGT
NM_012304.5:c.128-144142_128-144138delinsATAGT MANE Select	NP_036436.1:n.128-144142_128-144138delinsATAGT
NM_001278317.2:c.-14-144142_-14-144138delinsATAGT	NP_001265246.1:n.-14-144142_-14-144138delinsATAGT