Canonical Allele Identifier: CA410457061
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333168G>A , CM000683.2:g.44333168G>A GRCh38
NC_000021.8:g.45753051G>A , CM000683.1:g.45753051G>A GRCh37
NC_000021.7:g.44577479G>A NCBI36
NG_032952.1:g.11235C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.238C>T MANE Select ENSP00000344566.4:p.Leu80Phe
ENST00000325223.7:c.238C>T ENSP00000317302.7:p.Leu80Phe
ENST00000339818.8:c.238C>T ENSP00000344566.4:p.Leu80Phe
ENST00000397956.7:c.238C>T ENSP00000381047.3:p.Leu80Phe
ENST00000462742.1:n.2409C>T
ENST00000478674.1:n.297C>T
ENST00000496321.5:n.354C>T
NM_001271440.1:c.238C>T NP_001258369.1:p.Leu80Phe
NM_001271441.1:c.238C>T NP_001258370.1:p.Leu80Phe
NM_001271442.1:c.115C>T NP_001258371.1:p.Leu39Phe
NM_004928.2:c.238C>T NP_004919.1:p.Leu80Phe
XM_006724051.2:c.313C>T XP_006724114.1:p.Leu105Phe
XM_006724052.2:c.313C>T XP_006724115.1:p.Leu105Phe
XM_006724053.2:c.-87C>T XP_006724116.1:n.-87C>T
XR_937571.1:n.441C>T
XM_006724051.3:c.313C>T XP_006724114.1:p.Leu105Phe
XM_006724053.3:c.-87C>T XP_006724116.1:n.-87C>T
XM_017028470.1:c.442C>T XP_016883959.1:p.Leu148Phe
XM_017028471.1:c.187C>T XP_016883960.1:p.Leu63Phe
XM_017028472.1:c.-87C>T XP_016883961.1:n.-87C>T
XR_937571.2:n.448C>T
NM_004928.3:c.238C>T MANE Select NP_004919.1:p.Leu80Phe
NM_001271440.2:c.238C>T NP_001258369.1:p.Leu80Phe
NM_001271441.2:c.238C>T NP_001258370.1:p.Leu80Phe