Canonical Allele Identifier: CA2401985167
Gene: FBXO7 HGNC NCBI

Linked Data

dbSNP Id: rs2057416257

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474976_32474981dup , CM000684.2:g.32474976_32474981dup GRCh38
NC_000022.10:g.32870963_32870968dup , CM000684.1:g.32870963_32870968dup GRCh37
NC_000022.9:g.31200963_31200968dup NCBI36
NG_016001.1:g.5257_5262dup
NG_016001.2:g.5257_5262dup

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-27_-22dup MANE Select ENSP00000266087.7:n.-27_-22dup
ENST00000266087.11:c.-27_-22dup ENSP00000266087.7:n.-27_-22dup
ENST00000420700.5:c.-27_-22dup ENSP00000406155.1:n.-27_-22dup
ENST00000425028.5:c.-27_-22dup ENSP00000395823.1:n.-27_-22dup
NM_012179.3:c.-27_-22dup NP_036311.3:n.-27_-22dup
XM_011530106.1:c.-200_-195dup XP_011528408.1:n.-200_-195dup
XM_024452207.1:c.-217_-212dup XP_024307975.1:n.-217_-212dup
NM_012179.4:c.-27_-22dup MANE Select NP_036311.3:n.-27_-22dup