Canonical Allele Identifier: CA410457493
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333222G>C , CM000683.2:g.44333222G>C GRCh38
NC_000021.8:g.45753105G>C , CM000683.1:g.45753105G>C GRCh37
NC_000021.7:g.44577533G>C NCBI36
NG_032952.1:g.11181C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.184C>G MANE Select ENSP00000344566.4:p.Gln62Glu
ENST00000325223.7:c.184C>G ENSP00000317302.7:p.Gln62Glu
ENST00000339818.8:c.184C>G ENSP00000344566.4:p.Gln62Glu
ENST00000397956.7:c.184C>G ENSP00000381047.3:p.Gln62Glu
ENST00000462742.1:n.2355C>G
ENST00000478674.1:n.243C>G
ENST00000496321.5:n.300C>G
NM_001271440.1:c.184C>G NP_001258369.1:p.Gln62Glu
NM_001271441.1:c.184C>G NP_001258370.1:p.Gln62Glu
NM_001271442.1:c.61C>G NP_001258371.1:p.Gln21Glu
NM_004928.2:c.184C>G NP_004919.1:p.Gln62Glu
XM_006724051.2:c.259C>G XP_006724114.1:p.Gln87Glu
XM_006724052.2:c.259C>G XP_006724115.1:p.Gln87Glu
XM_006724053.2:c.-141C>G XP_006724116.1:n.-141C>G
XR_937571.1:n.387C>G
XM_006724051.3:c.259C>G XP_006724114.1:p.Gln87Glu
XM_006724053.3:c.-141C>G XP_006724116.1:n.-141C>G
XM_017028470.1:c.388C>G XP_016883959.1:p.Gln130Glu
XM_017028471.1:c.133C>G XP_016883960.1:p.Gln45Glu
XM_017028472.1:c.-141C>G XP_016883961.1:n.-141C>G
XR_937571.2:n.394C>G
NM_004928.3:c.184C>G MANE Select NP_004919.1:p.Gln62Glu
NM_001271440.2:c.184C>G NP_001258369.1:p.Gln62Glu
NM_001271441.2:c.184C>G NP_001258370.1:p.Gln62Glu