Canonical Allele Identifier: CA1529373299

Gene: FBXL7

Linked Data

• dbSNP Id: rs1737055424

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783566_15783568del , CM000667.2:g.15783566_15783568del	GRCh38
NC_000005.9:g.15783675_15783677del , CM000667.1:g.15783675_15783677del	GRCh37
NC_000005.8:g.15836675_15836677del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144324_128-144322del MANE Select	ENSP00000423630.1:n.128-144324_128-144322del
ENST00000504595.1:c.128-144324_128-144322del	ENSP00000423630.1:n.128-144324_128-144322del
ENST00000510662.1:c.-14-144324_-14-144322del	ENSP00000425184.1:n.-14-144324_-14-144322del
NM_001278317.1:c.-14-144324_-14-144322del	NP_001265246.1:n.-14-144324_-14-144322del
NM_012304.4:c.128-144324_128-144322del	NP_036436.1:n.128-144324_128-144322del
XM_005248273.3:c.113-144324_113-144322del	XP_005248330.1:n.113-144324_113-144322del
XM_011513998.1:c.-91-51211_-91-51209del	XP_011512300.1:n.-91-51211_-91-51209del
XM_017009262.2:c.113-144324_113-144322del	XP_016864751.1:n.113-144324_113-144322del
NM_012304.5:c.128-144324_128-144322del MANE Select	NP_036436.1:n.128-144324_128-144322del
NM_001278317.2:c.-14-144324_-14-144322del	NP_001265246.1:n.-14-144324_-14-144322del