Canonical Allele Identifier: CA2654807985
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333308_44333309del , CM000683.2:g.44333308_44333309del GRCh38
NC_000021.8:g.45753191_45753192del , CM000683.1:g.45753191_45753192del GRCh37
NC_000021.7:g.44577619_44577620del NCBI36
NG_032952.1:g.11097_11098del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.144-44_144-43del MANE Select ENSP00000344566.4:n.144-44_144-43del
ENST00000325223.7:c.144-44_144-43del ENSP00000317302.7:n.144-44_144-43del
ENST00000339818.8:c.144-44_144-43del ENSP00000344566.4:n.144-44_144-43del
ENST00000397956.7:c.144-44_144-43del ENSP00000381047.3:n.144-44_144-43del
ENST00000462742.1:n.2315-44_2315-43del
ENST00000478674.1:n.159_160del
ENST00000496321.5:n.269-53_269-52del
NM_001271440.1:c.144-44_144-43del NP_001258369.1:n.144-44_144-43del
NM_001271441.1:c.144-44_144-43del NP_001258370.1:n.144-44_144-43del
NM_001271442.1:c.30-53_30-52del NP_001258371.1:n.30-53_30-52del
NM_004928.2:c.144-44_144-43del NP_004919.1:n.144-44_144-43del
XM_006724051.2:c.219-44_219-43del XP_006724114.1:n.219-44_219-43del
XM_006724052.2:c.219-44_219-43del XP_006724115.1:n.219-44_219-43del
XM_006724053.2:c.-181-44_-181-43del XP_006724116.1:n.-181-44_-181-43del
XR_937571.1:n.347-44_347-43del
XM_006724051.3:c.219-44_219-43del XP_006724114.1:n.219-44_219-43del
XM_006724053.3:c.-181-44_-181-43del XP_006724116.1:n.-181-44_-181-43del
XM_017028470.1:c.348-44_348-43del XP_016883959.1:n.348-44_348-43del
XM_017028471.1:c.93-44_93-43del XP_016883960.1:n.93-44_93-43del
XM_017028472.1:c.-181-44_-181-43del XP_016883961.1:n.-181-44_-181-43del
XR_937571.2:n.354-44_354-43del
NM_004928.3:c.144-44_144-43del MANE Select NP_004919.1:n.144-44_144-43del
NM_001271440.2:c.144-44_144-43del NP_001258369.1:n.144-44_144-43del
NM_001271441.2:c.144-44_144-43del NP_001258370.1:n.144-44_144-43del