Canonical Allele Identifier: CA1073534352

Gene: FBXL7

Linked Data

• dbSNP Id: rs1737067288
• gnomAD v3: 5-15783915-C-CT
• gnomAD v4: 5-15783915-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783919dup , CM000667.2:g.15783919dup	GRCh38
NC_000005.9:g.15784028dup , CM000667.1:g.15784028dup	GRCh37
NC_000005.8:g.15837028dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-143971dup MANE Select	ENSP00000423630.1:n.128-143971dup
ENST00000504595.1:c.128-143971dup	ENSP00000423630.1:n.128-143971dup
ENST00000510662.1:c.-14-143971dup	ENSP00000425184.1:n.-14-143971dup
NM_001278317.1:c.-14-143971dup	NP_001265246.1:n.-14-143971dup
NM_012304.4:c.128-143971dup	NP_036436.1:n.128-143971dup
XM_005248273.3:c.113-143971dup	XP_005248330.1:n.113-143971dup
XM_011513998.1:c.-91-50858dup	XP_011512300.1:n.-91-50858dup
XM_017009262.2:c.113-143971dup	XP_016864751.1:n.113-143971dup
NM_012304.5:c.128-143971dup MANE Select	NP_036436.1:n.128-143971dup
NM_001278317.2:c.-14-143971dup	NP_001265246.1:n.-14-143971dup