Canonical Allele Identifier: CA2577621289
Gene: CFAP410 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333037del , CM000683.2:g.44333037del GRCh38
NC_000021.8:g.45752920del , CM000683.1:g.45752920del GRCh37
NC_000021.7:g.44577348del NCBI36
NG_032952.1:g.11367del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.370del MANE Select ENSP00000344566.4:p.Gln124ArgfsTer3
ENST00000325223.7:c.370del ENSP00000317302.7:p.Gln124ArgfsTer3
ENST00000339818.8:c.370del ENSP00000344566.4:p.Gln124ArgfsTer3
ENST00000397956.7:c.370del ENSP00000381047.3:p.Gln124ArgfsTer3
ENST00000462742.1:n.2541del
ENST00000478674.1:n.429del
ENST00000496321.5:n.486del
NM_001271440.1:c.370del NP_001258369.1:p.Gln124ArgfsTer3
NM_001271441.1:c.370del NP_001258370.1:p.Gln124ArgfsTer3
NM_001271442.1:c.247del NP_001258371.1:p.Gln83ArgfsTer3
NM_004928.2:c.370del NP_004919.1:p.Gln124ArgfsTer3
XM_006724051.2:c.445del XP_006724114.1:p.Gln149ArgfsTer3
XM_006724052.2:c.445del XP_006724115.1:p.Gln149ArgfsTer3
XM_006724053.2:c.46del XP_006724116.1:p.Gln16ArgfsTer3
XR_937571.1:n.573del
XM_006724051.3:c.445del XP_006724114.1:p.Gln149ArgfsTer3
XM_006724053.3:c.46del XP_006724116.1:p.Gln16ArgfsTer3
XM_017028470.1:c.574del XP_016883959.1:p.Gln192ArgfsTer3
XM_017028471.1:c.319del XP_016883960.1:p.Gln107ArgfsTer3
XM_017028472.1:c.46del XP_016883961.1:p.Gln16ArgfsTer3
XR_937571.2:n.580del
NM_004928.3:c.370del MANE Select NP_004919.1:p.Gln124ArgfsTer3
NM_001271440.2:c.370del NP_001258369.1:p.Gln124ArgfsTer3
NM_001271441.2:c.370del NP_001258370.1:p.Gln124ArgfsTer3