Canonical Allele Identifier: CA1073534139
Gene: FBXL7 HGNC NCBI

Linked Data

dbSNP Id: rs1737048849
gnomAD v3: 5-15783360-AC-A
gnomAD v4: 5-15783360-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783361del , CM000667.2:g.15783361del GRCh38
NC_000005.9:g.15783470del , CM000667.1:g.15783470del GRCh37
NC_000005.8:g.15836470del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504595.2:c.128-144529del MANE Select ENSP00000423630.1:n.128-144529del
ENST00000504595.1:c.128-144529del ENSP00000423630.1:n.128-144529del
ENST00000510662.1:c.-14-144529del ENSP00000425184.1:n.-14-144529del
NM_001278317.1:c.-14-144529del NP_001265246.1:n.-14-144529del
NM_012304.4:c.128-144529del NP_036436.1:n.128-144529del
XM_005248273.3:c.113-144529del XP_005248330.1:n.113-144529del
XM_011513998.1:c.-91-51416del XP_011512300.1:n.-91-51416del
XM_017009262.2:c.113-144529del XP_016864751.1:n.113-144529del
NM_012304.5:c.128-144529del MANE Select NP_036436.1:n.128-144529del
NM_001278317.2:c.-14-144529del NP_001265246.1:n.-14-144529del
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