Canonical Allele Identifier: CA411329998
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475103T>A , CM000684.2:g.32475103T>A GRCh38
NC_000022.10:g.32871090T>A , CM000684.1:g.32871090T>A GRCh37
NC_000022.9:g.31201090T>A NCBI36
NG_016001.1:g.5384T>A
NG_016001.2:g.5384T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.101T>A MANE Select ENSP00000266087.7:p.Leu34Gln
ENST00000266087.11:c.101T>A ENSP00000266087.7:p.Leu34Gln
ENST00000420700.5:c.101T>A ENSP00000406155.1:p.Leu34Gln
ENST00000425028.5:c.101T>A ENSP00000395823.1:p.Leu34Gln
ENST00000492535.1:n.89T>A
NM_012179.3:c.101T>A NP_036311.3:p.Leu34Gln
XM_011530106.1:c.-73T>A XP_011528408.1:n.-73T>A
XM_024452207.1:c.-90T>A XP_024307975.1:n.-90T>A
NM_012179.4:c.101T>A MANE Select NP_036311.3:p.Leu34Gln