Canonical Allele Identifier: CA2654807651
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44332866_44332886dup , CM000683.2:g.44332866_44332886dup GRCh38
NC_000021.8:g.45752749_45752769dup , CM000683.1:g.45752749_45752769dup GRCh37
NC_000021.7:g.44577177_44577197dup NCBI36
NG_032952.1:g.11519_11539dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.373+149_373+169dup MANE Select ENSP00000344566.4:n.373+149_373+169dup
ENST00000325223.7:c.373+149_373+169dup ENSP00000317302.7:n.373+149_373+169dup
ENST00000339818.8:c.373+149_373+169dup ENSP00000344566.4:n.373+149_373+169dup
ENST00000397956.7:c.373+149_373+169dup ENSP00000381047.3:n.373+149_373+169dup
ENST00000462742.1:n.2544+149_2544+169dup
ENST00000478674.1:n.432+149_432+169dup
ENST00000496321.5:n.489+149_489+169dup
NM_001271440.1:c.373+149_373+169dup NP_001258369.1:n.373+149_373+169dup
NM_001271441.1:c.373+149_373+169dup NP_001258370.1:n.373+149_373+169dup
NM_001271442.1:c.250+149_250+169dup NP_001258371.1:n.250+149_250+169dup
NM_004928.2:c.373+149_373+169dup NP_004919.1:n.373+149_373+169dup
XM_006724051.2:c.448+149_448+169dup XP_006724114.1:n.448+149_448+169dup
XM_006724052.2:c.448+149_448+169dup XP_006724115.1:n.448+149_448+169dup
XM_006724053.2:c.49+149_49+169dup XP_006724116.1:n.49+149_49+169dup
XR_937571.1:n.576+149_576+169dup
XM_006724051.3:c.448+149_448+169dup XP_006724114.1:n.448+149_448+169dup
XM_006724053.3:c.49+149_49+169dup XP_006724116.1:n.49+149_49+169dup
XM_017028470.1:c.577+149_577+169dup XP_016883959.1:n.577+149_577+169dup
XM_017028471.1:c.322+149_322+169dup XP_016883960.1:n.322+149_322+169dup
XM_017028472.1:c.49+149_49+169dup XP_016883961.1:n.49+149_49+169dup
XR_937571.2:n.583+149_583+169dup
NM_004928.3:c.373+149_373+169dup MANE Select NP_004919.1:n.373+149_373+169dup
NM_001271440.2:c.373+149_373+169dup NP_001258369.1:n.373+149_373+169dup
NM_001271441.2:c.373+149_373+169dup NP_001258370.1:n.373+149_373+169dup