Canonical Allele Identifier: CA4060474
Gene: FBXO5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.152975120C>G , CM000668.2:g.152975120C>G GRCh38
NC_000006.11:g.153296255C>G , CM000668.1:g.153296255C>G GRCh37
NC_000006.10:g.153337948C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_012177.5:c.605G>C MANE Select NP_036309.1:p.Cys202Ser
ENST00000229758.8:c.605G>C MANE Select ENSP00000229758.3:p.Cys202Ser
NM_001142522.1:c.467G>C NP_001135994.1:p.Cys156Ser
NM_001142522.2:c.467G>C NP_001135994.1:p.Cys156Ser
NM_001142522.3:c.467G>C NP_001135994.1:p.Cys156Ser
NM_012177.3:c.605G>C NP_036309.1:p.Cys202Ser
NM_012177.4:c.605G>C NP_036309.1:p.Cys202Ser
ENST00000229758.7:c.605G>C ENSP00000229758.3:p.Cys202Ser
ENST00000367241.3:c.467G>C ENSP00000356210.3:p.Cys156Ser
XM_011535749.1:c.620G>C XP_011534051.1:p.Cys207Ser