Canonical Allele Identifier: CA410456335
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333080A>T , CM000683.2:g.44333080A>T GRCh38
NC_000021.8:g.45752963A>T , CM000683.1:g.45752963A>T GRCh37
NC_000021.7:g.44577391A>T NCBI36
NG_032952.1:g.11323T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.326T>A MANE Select ENSP00000344566.4:p.Met109Lys
ENST00000325223.7:c.326T>A ENSP00000317302.7:p.Met109Lys
ENST00000339818.8:c.326T>A ENSP00000344566.4:p.Met109Lys
ENST00000397956.7:c.326T>A ENSP00000381047.3:p.Met109Lys
ENST00000462742.1:n.2497T>A
ENST00000478674.1:n.385T>A
ENST00000496321.5:n.442T>A
NM_001271440.1:c.326T>A NP_001258369.1:p.Met109Lys
NM_001271441.1:c.326T>A NP_001258370.1:p.Met109Lys
NM_001271442.1:c.203T>A NP_001258371.1:p.Met68Lys
NM_004928.2:c.326T>A NP_004919.1:p.Met109Lys
XM_006724051.2:c.401T>A XP_006724114.1:p.Met134Lys
XM_006724052.2:c.401T>A XP_006724115.1:p.Met134Lys
XM_006724053.2:c.2T>A XP_006724116.1:p.Met1Lys
XR_937571.1:n.529T>A
XM_006724051.3:c.401T>A XP_006724114.1:p.Met134Lys
XM_006724053.3:c.2T>A XP_006724116.1:p.Met1Lys
XM_017028470.1:c.530T>A XP_016883959.1:p.Met177Lys
XM_017028471.1:c.275T>A XP_016883960.1:p.Met92Lys
XM_017028472.1:c.2T>A XP_016883961.1:p.Met1Lys
XR_937571.2:n.536T>A
NM_004928.3:c.326T>A MANE Select NP_004919.1:p.Met109Lys
NM_001271440.2:c.326T>A NP_001258369.1:p.Met109Lys
NM_001271441.2:c.326T>A NP_001258370.1:p.Met109Lys