Canonical Allele Identifier: CA2391590911
Gene: CFAP410 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333049C= , CM000683.2:g.44333049C= GRCh38
NC_000021.8:g.45752932C= , CM000683.1:g.45752932C= GRCh37
NC_000021.7:g.44577360C= NCBI36
NG_032952.1:g.11354G=

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.357G= MANE Select ENSP00000344566.4:p.Gln119=
ENST00000325223.7:c.357G= ENSP00000317302.7:p.Gln119=
ENST00000339818.8:c.357G= ENSP00000344566.4:p.Gln119=
ENST00000397956.7:c.357G= ENSP00000381047.3:p.Gln119=
ENST00000462742.1:n.2528G=
ENST00000478674.1:n.416G=
ENST00000496321.5:n.473G=
NM_001271440.1:c.357G= NP_001258369.1:p.Gln119=
NM_001271441.1:c.357G= NP_001258370.1:p.Gln119=
NM_001271442.1:c.234G= NP_001258371.1:p.Gln78=
NM_004928.2:c.357G= NP_004919.1:p.Gln119=
XM_006724051.2:c.432G= XP_006724114.1:p.Gln144=
XM_006724052.2:c.432G= XP_006724115.1:p.Gln144=
XM_006724053.2:c.33G= XP_006724116.1:p.Gln11=
XR_937571.1:n.560G=
XM_006724051.3:c.432G= XP_006724114.1:p.Gln144=
XM_006724053.3:c.33G= XP_006724116.1:p.Gln11=
XM_017028470.1:c.561G= XP_016883959.1:p.Gln187=
XM_017028471.1:c.306G= XP_016883960.1:p.Gln102=
XM_017028472.1:c.33G= XP_016883961.1:p.Gln11=
XR_937571.2:n.567G=
NM_004928.3:c.357G= MANE Select NP_004919.1:p.Gln119=
NM_001271440.2:c.357G= NP_001258369.1:p.Gln119=
NM_001271441.2:c.357G= NP_001258370.1:p.Gln119=