Canonical Allele Identifier: CA410457104
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333173G>T , CM000683.2:g.44333173G>T GRCh38
NC_000021.8:g.45753056G>T , CM000683.1:g.45753056G>T GRCh37
NC_000021.7:g.44577484G>T NCBI36
NG_032952.1:g.11230C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.233C>A MANE Select ENSP00000344566.4:p.Ala78Asp
ENST00000325223.7:c.233C>A ENSP00000317302.7:p.Ala78Asp
ENST00000339818.8:c.233C>A ENSP00000344566.4:p.Ala78Asp
ENST00000397956.7:c.233C>A ENSP00000381047.3:p.Ala78Asp
ENST00000462742.1:n.2404C>A
ENST00000478674.1:n.292C>A
ENST00000496321.5:n.349C>A
NM_001271440.1:c.233C>A NP_001258369.1:p.Ala78Asp
NM_001271441.1:c.233C>A NP_001258370.1:p.Ala78Asp
NM_001271442.1:c.110C>A NP_001258371.1:p.Ala37Asp
NM_004928.2:c.233C>A NP_004919.1:p.Ala78Asp
XM_006724051.2:c.308C>A XP_006724114.1:p.Ala103Asp
XM_006724052.2:c.308C>A XP_006724115.1:p.Ala103Asp
XM_006724053.2:c.-92C>A XP_006724116.1:n.-92C>A
XR_937571.1:n.436C>A
XM_006724051.3:c.308C>A XP_006724114.1:p.Ala103Asp
XM_006724053.3:c.-92C>A XP_006724116.1:n.-92C>A
XM_017028470.1:c.437C>A XP_016883959.1:p.Ala146Asp
XM_017028471.1:c.182C>A XP_016883960.1:p.Ala61Asp
XM_017028472.1:c.-92C>A XP_016883961.1:n.-92C>A
XR_937571.2:n.443C>A
NM_004928.3:c.233C>A MANE Select NP_004919.1:p.Ala78Asp
NM_001271440.2:c.233C>A NP_001258369.1:p.Ala78Asp
NM_001271441.2:c.233C>A NP_001258370.1:p.Ala78Asp