Canonical Allele Identifier: CA639098925
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs1464219550
gnomAD v2: 22-32870954-T-TCCGGGTCCAGGCCCCTCGGGCCGCCTGCCG
gnomAD v4: 22-32474967-T-TCCGGGTCCAGGCCCCTCGGGCCGCCTGCCG
MyVariant Identifiers: chr22:g.32870954_32870955insCCGGGTCCAGGCCCCTCGGGCCGCCTGCCG (hg19) chr22:g.32474967_32474968insCCGGGTCCAGGCCCCTCGGGCCGCCTGCCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474971_32475000dup , CM000684.2:g.32474971_32475000dup GRCh38
NC_000022.10:g.32870958_32870987dup , CM000684.1:g.32870958_32870987dup GRCh37
NC_000022.9:g.31200958_31200987dup NCBI36
NG_016001.1:g.5252_5281dup
NG_016001.2:g.5252_5281dup

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-32_-3dup MANE Select ENSP00000266087.7:n.-32_-3dup
ENST00000266087.11:c.-32_-3dup ENSP00000266087.7:n.-32_-3dup
ENST00000420700.5:c.-32_-3dup ENSP00000406155.1:n.-32_-3dup
ENST00000425028.5:c.-32_-3dup ENSP00000395823.1:n.-32_-3dup
NM_012179.3:c.-32_-3dup NP_036311.3:n.-32_-3dup
XM_011530106.1:c.-205_-176dup XP_011528408.1:n.-205_-176dup
XM_024452207.1:c.-222_-193dup XP_024307975.1:n.-222_-193dup
NM_012179.4:c.-32_-3dup MANE Select NP_036311.3:n.-32_-3dup
Search 100 bp 5'
Search 100 bp 3'