Canonical Allele Identifier: CA2401985165
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474972G= , CM000684.2:g.32474972G= GRCh38
NC_000022.10:g.32870959G= , CM000684.1:g.32870959G= GRCh37
NC_000022.9:g.31200959G= NCBI36
NG_016001.1:g.5253G=
NG_016001.2:g.5253G=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-31G= MANE Select ENSP00000266087.7:n.-31G=
ENST00000266087.11:c.-31G= ENSP00000266087.7:n.-31G=
ENST00000420700.5:c.-31G= ENSP00000406155.1:n.-31G=
ENST00000425028.5:c.-31G= ENSP00000395823.1:n.-31G=
NM_012179.3:c.-31G= NP_036311.3:n.-31G=
XM_011530106.1:c.-204G= XP_011528408.1:n.-204G=
XM_024452207.1:c.-221G= XP_024307975.1:n.-221G=
NM_012179.4:c.-31G= MANE Select NP_036311.3:n.-31G=