Canonical Allele Identifier: CA2401985169
Gene: FBXO7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32474976A= , CM000684.2:g.32474976A= GRCh38
NC_000022.10:g.32870963A= , CM000684.1:g.32870963A= GRCh37
NC_000022.9:g.31200963A= NCBI36
NG_016001.1:g.5257A=
NG_016001.2:g.5257A=

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.-27A= MANE Select ENSP00000266087.7:n.-27A=
ENST00000266087.11:c.-27A= ENSP00000266087.7:n.-27A=
ENST00000420700.5:c.-27A= ENSP00000406155.1:n.-27A=
ENST00000425028.5:c.-27A= ENSP00000395823.1:n.-27A=
NM_012179.3:c.-27A= NP_036311.3:n.-27A=
XM_011530106.1:c.-200A= XP_011528408.1:n.-200A=
XM_024452207.1:c.-217A= XP_024307975.1:n.-217A=
NM_012179.4:c.-27A= MANE Select NP_036311.3:n.-27A=