Canonical Allele Identifier: CA410456572
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333111A>C , CM000683.2:g.44333111A>C GRCh38
NC_000021.8:g.45752994A>C , CM000683.1:g.45752994A>C GRCh37
NC_000021.7:g.44577422A>C NCBI36
NG_032952.1:g.11292T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.295T>G MANE Select ENSP00000344566.4:p.Cys99Gly
ENST00000325223.7:c.295T>G ENSP00000317302.7:p.Cys99Gly
ENST00000339818.8:c.295T>G ENSP00000344566.4:p.Cys99Gly
ENST00000397956.7:c.295T>G ENSP00000381047.3:p.Cys99Gly
ENST00000462742.1:n.2466T>G
ENST00000478674.1:n.354T>G
ENST00000496321.5:n.411T>G
NM_001271440.1:c.295T>G NP_001258369.1:p.Cys99Gly
NM_001271441.1:c.295T>G NP_001258370.1:p.Cys99Gly
NM_001271442.1:c.172T>G NP_001258371.1:p.Cys58Gly
NM_004928.2:c.295T>G NP_004919.1:p.Cys99Gly
XM_006724051.2:c.370T>G XP_006724114.1:p.Cys124Gly
XM_006724052.2:c.370T>G XP_006724115.1:p.Cys124Gly
XM_006724053.2:c.-30T>G XP_006724116.1:n.-30T>G
XR_937571.1:n.498T>G
XM_006724051.3:c.370T>G XP_006724114.1:p.Cys124Gly
XM_006724053.3:c.-30T>G XP_006724116.1:n.-30T>G
XM_017028470.1:c.499T>G XP_016883959.1:p.Cys167Gly
XM_017028471.1:c.244T>G XP_016883960.1:p.Cys82Gly
XM_017028472.1:c.-30T>G XP_016883961.1:n.-30T>G
XR_937571.2:n.505T>G
NM_004928.3:c.295T>G MANE Select NP_004919.1:p.Cys99Gly
NM_001271440.2:c.295T>G NP_001258369.1:p.Cys99Gly
NM_001271441.2:c.295T>G NP_001258370.1:p.Cys99Gly