Canonical Allele Identifier: CA410456364
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333086T>A , CM000683.2:g.44333086T>A GRCh38
NC_000021.8:g.45752969T>A , CM000683.1:g.45752969T>A GRCh37
NC_000021.7:g.44577397T>A NCBI36
NG_032952.1:g.11317A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.320A>T MANE Select ENSP00000344566.4:p.Tyr107Phe
ENST00000325223.7:c.320A>T ENSP00000317302.7:p.Tyr107Phe
ENST00000339818.8:c.320A>T ENSP00000344566.4:p.Tyr107Phe
ENST00000397956.7:c.320A>T ENSP00000381047.3:p.Tyr107Phe
ENST00000462742.1:n.2491A>T
ENST00000478674.1:n.379A>T
ENST00000496321.5:n.436A>T
NM_001271440.1:c.320A>T NP_001258369.1:p.Tyr107Phe
NM_001271441.1:c.320A>T NP_001258370.1:p.Tyr107Phe
NM_001271442.1:c.197A>T NP_001258371.1:p.Tyr66Phe
NM_004928.2:c.320A>T NP_004919.1:p.Tyr107Phe
XM_006724051.2:c.395A>T XP_006724114.1:p.Tyr132Phe
XM_006724052.2:c.395A>T XP_006724115.1:p.Tyr132Phe
XM_006724053.2:c.-5A>T XP_006724116.1:n.-5A>T
XR_937571.1:n.523A>T
XM_006724051.3:c.395A>T XP_006724114.1:p.Tyr132Phe
XM_006724053.3:c.-5A>T XP_006724116.1:n.-5A>T
XM_017028470.1:c.524A>T XP_016883959.1:p.Tyr175Phe
XM_017028471.1:c.269A>T XP_016883960.1:p.Tyr90Phe
XM_017028472.1:c.-5A>T XP_016883961.1:n.-5A>T
XR_937571.2:n.530A>T
NM_004928.3:c.320A>T MANE Select NP_004919.1:p.Tyr107Phe
NM_001271440.2:c.320A>T NP_001258369.1:p.Tyr107Phe
NM_001271441.2:c.320A>T NP_001258370.1:p.Tyr107Phe