Canonical Allele Identifier: CA410456230
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333057G>C , CM000683.2:g.44333057G>C GRCh38
NC_000021.8:g.45752940G>C , CM000683.1:g.45752940G>C GRCh37
NC_000021.7:g.44577368G>C NCBI36
NG_032952.1:g.11346C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.349C>G MANE Select ENSP00000344566.4:p.Arg117Gly
ENST00000325223.7:c.349C>G ENSP00000317302.7:p.Arg117Gly
ENST00000339818.8:c.349C>G ENSP00000344566.4:p.Arg117Gly
ENST00000397956.7:c.349C>G ENSP00000381047.3:p.Arg117Gly
ENST00000462742.1:n.2520C>G
ENST00000478674.1:n.408C>G
ENST00000496321.5:n.465C>G
NM_001271440.1:c.349C>G NP_001258369.1:p.Arg117Gly
NM_001271441.1:c.349C>G NP_001258370.1:p.Arg117Gly
NM_001271442.1:c.226C>G NP_001258371.1:p.Arg76Gly
NM_004928.2:c.349C>G NP_004919.1:p.Arg117Gly
XM_006724051.2:c.424C>G XP_006724114.1:p.Arg142Gly
XM_006724052.2:c.424C>G XP_006724115.1:p.Arg142Gly
XM_006724053.2:c.25C>G XP_006724116.1:p.Arg9Gly
XR_937571.1:n.552C>G
XM_006724051.3:c.424C>G XP_006724114.1:p.Arg142Gly
XM_006724053.3:c.25C>G XP_006724116.1:p.Arg9Gly
XM_017028470.1:c.553C>G XP_016883959.1:p.Arg185Gly
XM_017028471.1:c.298C>G XP_016883960.1:p.Arg100Gly
XM_017028472.1:c.25C>G XP_016883961.1:p.Arg9Gly
XR_937571.2:n.559C>G
NM_004928.3:c.349C>G MANE Select NP_004919.1:p.Arg117Gly
NM_001271440.2:c.349C>G NP_001258369.1:p.Arg117Gly
NM_001271441.2:c.349C>G NP_001258370.1:p.Arg117Gly