Canonical Allele Identifier: CA2656311522
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475163_32475169del , CM000684.2:g.32475163_32475169del GRCh38
NC_000022.10:g.32871150_32871156del , CM000684.1:g.32871150_32871156del GRCh37
NC_000022.9:g.31201150_31201156del NCBI36
NG_016001.1:g.5444_5450del
NG_016001.2:g.5444_5450del

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.122+39_122+45del MANE Select ENSP00000266087.7:n.122+39_122+45del
ENST00000266087.11:c.122+39_122+45del ENSP00000266087.7:n.122+39_122+45del
ENST00000420700.5:c.122+39_122+45del ENSP00000406155.1:n.122+39_122+45del
ENST00000425028.5:c.122+39_122+45del ENSP00000395823.1:n.122+39_122+45del
ENST00000492535.1:n.110+39_110+45del
NM_012179.3:c.122+39_122+45del NP_036311.3:n.122+39_122+45del
XM_011530106.1:c.-52+39_-52+45del XP_011528408.1:n.-52+39_-52+45del
XM_024452207.1:c.-69+39_-69+45del XP_024307975.1:n.-69+39_-69+45del
NM_012179.4:c.122+39_122+45del MANE Select NP_036311.3:n.122+39_122+45del