Canonical Allele Identifier: CA2654807978
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333307_44333315del , CM000683.2:g.44333307_44333315del GRCh38
NC_000021.8:g.45753190_45753198del , CM000683.1:g.45753190_45753198del GRCh37
NC_000021.7:g.44577618_44577626del NCBI36
NG_032952.1:g.11096_11104del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.144-45_144-37del MANE Select ENSP00000344566.4:n.144-45_144-37del
ENST00000325223.7:c.144-45_144-37del ENSP00000317302.7:n.144-45_144-37del
ENST00000339818.8:c.144-45_144-37del ENSP00000344566.4:n.144-45_144-37del
ENST00000397956.7:c.144-45_144-37del ENSP00000381047.3:n.144-45_144-37del
ENST00000462742.1:n.2315-45_2315-37del
ENST00000478674.1:n.158_166del
ENST00000496321.5:n.269-54_269-46del
NM_001271440.1:c.144-45_144-37del NP_001258369.1:n.144-45_144-37del
NM_001271441.1:c.144-45_144-37del NP_001258370.1:n.144-45_144-37del
NM_001271442.1:c.30-54_30-46del NP_001258371.1:n.30-54_30-46del
NM_004928.2:c.144-45_144-37del NP_004919.1:n.144-45_144-37del
XM_006724051.2:c.219-45_219-37del XP_006724114.1:n.219-45_219-37del
XM_006724052.2:c.219-45_219-37del XP_006724115.1:n.219-45_219-37del
XM_006724053.2:c.-181-45_-181-37del XP_006724116.1:n.-181-45_-181-37del
XR_937571.1:n.347-45_347-37del
XM_006724051.3:c.219-45_219-37del XP_006724114.1:n.219-45_219-37del
XM_006724053.3:c.-181-45_-181-37del XP_006724116.1:n.-181-45_-181-37del
XM_017028470.1:c.348-45_348-37del XP_016883959.1:n.348-45_348-37del
XM_017028471.1:c.93-45_93-37del XP_016883960.1:n.93-45_93-37del
XM_017028472.1:c.-181-45_-181-37del XP_016883961.1:n.-181-45_-181-37del
XR_937571.2:n.354-45_354-37del
NM_004928.3:c.144-45_144-37del MANE Select NP_004919.1:n.144-45_144-37del
NM_001271440.2:c.144-45_144-37del NP_001258369.1:n.144-45_144-37del
NM_001271441.2:c.144-45_144-37del NP_001258370.1:n.144-45_144-37del