Canonical Allele Identifier: CA366219026
Gene: FBXO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152975121A>T , CM000668.2:g.152975121A>T GRCh38
NC_000006.11:g.153296256A>T , CM000668.1:g.153296256A>T GRCh37
NC_000006.10:g.153337949A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_012177.5:c.604T>A MANE Select NP_036309.1:p.Cys202Ser
ENST00000229758.8:c.604T>A MANE Select ENSP00000229758.3:p.Cys202Ser
NM_001142522.1:c.466T>A NP_001135994.1:p.Cys156Ser
NM_001142522.2:c.466T>A NP_001135994.1:p.Cys156Ser
NM_001142522.3:c.466T>A NP_001135994.1:p.Cys156Ser
NM_012177.3:c.604T>A NP_036309.1:p.Cys202Ser
NM_012177.4:c.604T>A NP_036309.1:p.Cys202Ser
ENST00000229758.7:c.604T>A ENSP00000229758.3:p.Cys202Ser
ENST00000367241.3:c.466T>A ENSP00000356210.3:p.Cys156Ser
XM_011535749.1:c.619T>A XP_011534051.1:p.Cys207Ser