Canonical Allele Identifier: CA411329999
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.101T>C MANE Select ENSP00000266087.7:p.Leu34Pro
ENST00000266087.11:c.101T>C ENSP00000266087.7:p.Leu34Pro
ENST00000420700.5:c.101T>C ENSP00000406155.1:p.Leu34Pro
ENST00000425028.5:c.101T>C ENSP00000395823.1:p.Leu34Pro
ENST00000492535.1:n.89T>C
NM_012179.3:c.101T>C NP_036311.3:p.Leu34Pro
XM_011530106.1:c.-73T>C XP_011528408.1:n.-73T>C
XM_024452207.1:c.-90T>C XP_024307975.1:n.-90T>C
NM_012179.4:c.101T>C MANE Select NP_036311.3:p.Leu34Pro