Canonical Allele Identifier: CA411329813
Gene: FBXO7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.32475013G>T , CM000684.2:g.32475013G>T GRCh38
NC_000022.10:g.32871000G>T , CM000684.1:g.32871000G>T GRCh37
NC_000022.9:g.31201000G>T NCBI36
NG_016001.1:g.5294G>T
NG_016001.2:g.5294G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266087.12:c.11G>T MANE Select ENSP00000266087.7:p.Arg4Leu
ENST00000266087.11:c.11G>T ENSP00000266087.7:p.Arg4Leu
ENST00000420700.5:c.11G>T ENSP00000406155.1:p.Arg4Leu
ENST00000425028.5:c.11G>T ENSP00000395823.1:p.Arg4Leu
NM_012179.3:c.11G>T NP_036311.3:p.Arg4Leu
XM_011530106.1:c.-163G>T XP_011528408.1:n.-163G>T
XM_024452207.1:c.-180G>T XP_024307975.1:n.-180G>T
NM_012179.4:c.11G>T MANE Select NP_036311.3:p.Arg4Leu