Canonical Allele Identifier: CA411329951
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475080G>C , CM000684.2:g.32475080G>C GRCh38
NC_000022.10:g.32871067G>C , CM000684.1:g.32871067G>C GRCh37
NC_000022.9:g.31201067G>C NCBI36
NG_016001.1:g.5361G>C
NG_016001.2:g.5361G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266087.12:c.78G>C MANE Select ENSP00000266087.7:p.Leu26Phe
ENST00000266087.11:c.78G>C ENSP00000266087.7:p.Leu26Phe
ENST00000420700.5:c.78G>C ENSP00000406155.1:p.Leu26Phe
ENST00000425028.5:c.78G>C ENSP00000395823.1:p.Leu26Phe
ENST00000492535.1:n.66G>C
NM_012179.3:c.78G>C NP_036311.3:p.Leu26Phe
XM_011530106.1:c.-96G>C XP_011528408.1:n.-96G>C
XM_024452207.1:c.-113G>C XP_024307975.1:n.-113G>C
NM_012179.4:c.78G>C MANE Select NP_036311.3:p.Leu26Phe