Canonical Allele Identifier: CA1529373239

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783431_15783433delinsATA , CM000667.2:g.15783431_15783433delinsATA	GRCh38
NC_000005.9:g.15783540_15783542delinsATA , CM000667.1:g.15783540_15783542delinsATA	GRCh37
NC_000005.8:g.15836540_15836542delinsATA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144459_128-144457delinsATA MANE Select	ENSP00000423630.1:n.128-144459_128-144457delinsATA
ENST00000504595.1:c.128-144459_128-144457delinsATA	ENSP00000423630.1:n.128-144459_128-144457delinsATA
ENST00000510662.1:c.-14-144459_-14-144457delinsATA	ENSP00000425184.1:n.-14-144459_-14-144457delinsATA
NM_001278317.1:c.-14-144459_-14-144457delinsATA	NP_001265246.1:n.-14-144459_-14-144457delinsATA
NM_012304.4:c.128-144459_128-144457delinsATA	NP_036436.1:n.128-144459_128-144457delinsATA
XM_005248273.3:c.113-144459_113-144457delinsATA	XP_005248330.1:n.113-144459_113-144457delinsATA
XM_011513998.1:c.-91-51346_-91-51344delinsATA	XP_011512300.1:n.-91-51346_-91-51344delinsATA
XM_017009262.2:c.113-144459_113-144457delinsATA	XP_016864751.1:n.113-144459_113-144457delinsATA
NM_012304.5:c.128-144459_128-144457delinsATA MANE Select	NP_036436.1:n.128-144459_128-144457delinsATA
NM_001278317.2:c.-14-144459_-14-144457delinsATA	NP_001265246.1:n.-14-144459_-14-144457delinsATA