Canonical Allele Identifier: CA2401985181
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474991C= , CM000684.2:g.32474991C= GRCh38
NC_000022.10:g.32870978C= , CM000684.1:g.32870978C= GRCh37
NC_000022.9:g.31200978C= NCBI36
NG_016001.1:g.5272C=
NG_016001.2:g.5272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.-12C= MANE Select ENSP00000266087.7:n.-12C=
ENST00000266087.11:c.-12C= ENSP00000266087.7:n.-12C=
ENST00000420700.5:c.-12C= ENSP00000406155.1:n.-12C=
ENST00000425028.5:c.-12C= ENSP00000395823.1:n.-12C=
NM_012179.3:c.-12C= NP_036311.3:n.-12C=
XM_011530106.1:c.-185C= XP_011528408.1:n.-185C=
XM_024452207.1:c.-202C= XP_024307975.1:n.-202C=
NM_012179.4:c.-12C= MANE Select NP_036311.3:n.-12C=