Canonical Allele Identifier: CA1529373420

Gene: FBXL7

Linked Data

• dbSNP Id: rs1737062606

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783789_15783791del , CM000667.2:g.15783789_15783791del	GRCh38
NC_000005.9:g.15783898_15783900del , CM000667.1:g.15783898_15783900del	GRCh37
NC_000005.8:g.15836898_15836900del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144101_128-144099del MANE Select	ENSP00000423630.1:n.128-144101_128-144099del
ENST00000504595.1:c.128-144101_128-144099del	ENSP00000423630.1:n.128-144101_128-144099del
ENST00000510662.1:c.-14-144101_-14-144099del	ENSP00000425184.1:n.-14-144101_-14-144099del
NM_001278317.1:c.-14-144101_-14-144099del	NP_001265246.1:n.-14-144101_-14-144099del
NM_012304.4:c.128-144101_128-144099del	NP_036436.1:n.128-144101_128-144099del
XM_005248273.3:c.113-144101_113-144099del	XP_005248330.1:n.113-144101_113-144099del
XM_011513998.1:c.-91-50988_-91-50986del	XP_011512300.1:n.-91-50988_-91-50986del
XM_017009262.2:c.113-144101_113-144099del	XP_016864751.1:n.113-144101_113-144099del
NM_012304.5:c.128-144101_128-144099del MANE Select	NP_036436.1:n.128-144101_128-144099del
NM_001278317.2:c.-14-144101_-14-144099del	NP_001265246.1:n.-14-144101_-14-144099del