Canonical Allele Identifier: CA2391590971
Gene: CFAP410 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333140A= , CM000683.2:g.44333140A= GRCh38
NC_000021.8:g.45753023A= , CM000683.1:g.45753023A= GRCh37
NC_000021.7:g.44577451A= NCBI36
NG_032952.1:g.11263T=

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.266T= MANE Select ENSP00000344566.4:p.Leu89=
ENST00000325223.7:c.266T= ENSP00000317302.7:p.Leu89=
ENST00000339818.8:c.266T= ENSP00000344566.4:p.Leu89=
ENST00000397956.7:c.266T= ENSP00000381047.3:p.Leu89=
ENST00000462742.1:n.2437T=
ENST00000478674.1:n.325T=
ENST00000496321.5:n.382T=
NM_001271440.1:c.266T= NP_001258369.1:p.Leu89=
NM_001271441.1:c.266T= NP_001258370.1:p.Leu89=
NM_001271442.1:c.143T= NP_001258371.1:p.Leu48=
NM_004928.2:c.266T= NP_004919.1:p.Leu89=
XM_006724051.2:c.341T= XP_006724114.1:p.Leu114=
XM_006724052.2:c.341T= XP_006724115.1:p.Leu114=
XM_006724053.2:c.-59T= XP_006724116.1:n.-59T=
XR_937571.1:n.469T=
XM_006724051.3:c.341T= XP_006724114.1:p.Leu114=
XM_006724053.3:c.-59T= XP_006724116.1:n.-59T=
XM_017028470.1:c.470T= XP_016883959.1:p.Leu157=
XM_017028471.1:c.215T= XP_016883960.1:p.Leu72=
XM_017028472.1:c.-59T= XP_016883961.1:n.-59T=
XR_937571.2:n.476T=
NM_004928.3:c.266T= MANE Select NP_004919.1:p.Leu89=
NM_001271440.2:c.266T= NP_001258369.1:p.Leu89=
NM_001271441.2:c.266T= NP_001258370.1:p.Leu89=