Canonical Allele Identifier: CA2401985190
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475004T= , CM000684.2:g.32475004T= GRCh38
NC_000022.10:g.32870991T= , CM000684.1:g.32870991T= GRCh37
NC_000022.9:g.31200991T= NCBI36
NG_016001.1:g.5285T=
NG_016001.2:g.5285T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.2T= MANE Select ENSP00000266087.7:p.Met1=
ENST00000266087.11:c.2T= ENSP00000266087.7:p.Met1=
ENST00000420700.5:c.2T= ENSP00000406155.1:p.Met1=
ENST00000425028.5:c.2T= ENSP00000395823.1:p.Met1=
NM_012179.3:c.2T= NP_036311.3:p.Met1=
XM_011530106.1:c.-172T= XP_011528408.1:n.-172T=
XM_024452207.1:c.-189T= XP_024307975.1:n.-189T=
NM_012179.4:c.2T= MANE Select NP_036311.3:p.Met1=