Canonical Allele Identifier: CA2401985117
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474922T= , CM000684.2:g.32474922T= GRCh38
NC_000022.10:g.32870909T= , CM000684.1:g.32870909T= GRCh37
NC_000022.9:g.31200909T= NCBI36
NG_016001.1:g.5203T=
NG_016001.2:g.5203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-81T= MANE Select ENSP00000266087.7:n.-81T=
ENST00000266087.11:c.-81T= ENSP00000266087.7:n.-81T=
ENST00000420700.5:c.-81T= ENSP00000406155.1:n.-81T=
ENST00000425028.5:c.-81T= ENSP00000395823.1:n.-81T=
NM_012179.3:c.-81T= NP_036311.3:n.-81T=
XM_011530106.1:c.-254T= XP_011528408.1:n.-254T=
XM_024452207.1:c.-271T= XP_024307975.1:n.-271T=
NM_012179.4:c.-81T= MANE Select NP_036311.3:n.-81T=