Canonical Allele Identifier: CA806217973

Gene: FBXL7

Linked Data

• dbSNP Id: rs1208005837
• gnomAD v3: 5-15783788-TATTG-T
• gnomAD v4: 5-15783788-TATTG-T
• MyVariant Identifiers: chr5:g.15783898_15783901del (hg19) ; chr5:g.15783789_15783792del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783794_15783797del , CM000667.2:g.15783794_15783797del	GRCh38
NC_000005.9:g.15783903_15783906del , CM000667.1:g.15783903_15783906del	GRCh37
NC_000005.8:g.15836903_15836906del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.128-144096_128-144093del MANE Select	ENSP00000423630.1:n.128-144096_128-144093del
ENST00000504595.1:c.128-144096_128-144093del	ENSP00000423630.1:n.128-144096_128-144093del
ENST00000510662.1:c.-14-144096_-14-144093del	ENSP00000425184.1:n.-14-144096_-14-144093del
NM_001278317.1:c.-14-144096_-14-144093del	NP_001265246.1:n.-14-144096_-14-144093del
NM_012304.4:c.128-144096_128-144093del	NP_036436.1:n.128-144096_128-144093del
XM_005248273.3:c.113-144096_113-144093del	XP_005248330.1:n.113-144096_113-144093del
XM_011513998.1:c.-91-50983_-91-50980del	XP_011512300.1:n.-91-50983_-91-50980del
XM_017009262.2:c.113-144096_113-144093del	XP_016864751.1:n.113-144096_113-144093del
NM_012304.5:c.128-144096_128-144093del MANE Select	NP_036436.1:n.128-144096_128-144093del
NM_001278317.2:c.-14-144096_-14-144093del	NP_001265246.1:n.-14-144096_-14-144093del