Canonical Allele Identifier: CA2591123693
Gene: CFAP410 HGNC NCBI

Linked Data

dbSNP Id: rs2146066541

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44332753_44332755del , CM000683.2:g.44332753_44332755del GRCh38
NC_000021.8:g.45752636_45752638del , CM000683.1:g.45752636_45752638del GRCh37
NC_000021.7:g.44577064_44577066del NCBI36
NG_032952.1:g.11651_11653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.373+281_373+283del MANE Select ENSP00000344566.4:n.373+281_373+283del
ENST00000325223.7:c.373+281_373+283del ENSP00000317302.7:n.373+281_373+283del
ENST00000339818.8:c.373+281_373+283del ENSP00000344566.4:n.373+281_373+283del
ENST00000397956.7:c.373+281_373+283del ENSP00000381047.3:n.373+281_373+283del
ENST00000462742.1:n.2544+281_2544+283del
ENST00000478674.1:n.432+281_432+283del
ENST00000496321.5:n.489+281_489+283del
NM_001271440.1:c.373+281_373+283del NP_001258369.1:n.373+281_373+283del
NM_001271441.1:c.373+281_373+283del NP_001258370.1:n.373+281_373+283del
NM_001271442.1:c.250+281_250+283del NP_001258371.1:n.250+281_250+283del
NM_004928.2:c.373+281_373+283del NP_004919.1:n.373+281_373+283del
XM_006724051.2:c.448+281_448+283del XP_006724114.1:n.448+281_448+283del
XM_006724052.2:c.448+281_448+283del XP_006724115.1:n.448+281_448+283del
XM_006724053.2:c.49+281_49+283del XP_006724116.1:n.49+281_49+283del
XR_937571.1:n.576+281_576+283del
XM_006724051.3:c.448+281_448+283del XP_006724114.1:n.448+281_448+283del
XM_006724053.3:c.49+281_49+283del XP_006724116.1:n.49+281_49+283del
XM_017028470.1:c.577+281_577+283del XP_016883959.1:n.577+281_577+283del
XM_017028471.1:c.322+281_322+283del XP_016883960.1:n.322+281_322+283del
XM_017028472.1:c.49+281_49+283del XP_016883961.1:n.49+281_49+283del
XR_937571.2:n.583+281_583+283del
NM_004928.3:c.373+281_373+283del MANE Select NP_004919.1:n.373+281_373+283del
NM_001271440.2:c.373+281_373+283del NP_001258369.1:n.373+281_373+283del
NM_001271441.2:c.373+281_373+283del NP_001258370.1:n.373+281_373+283del