Canonical Allele Identifier: CA410457320
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333206A>C , CM000683.2:g.44333206A>C GRCh38
NC_000021.8:g.45753089A>C , CM000683.1:g.45753089A>C GRCh37
NC_000021.7:g.44577517A>C NCBI36
NG_032952.1:g.11197T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.200T>G MANE Select ENSP00000344566.4:p.Leu67Arg
ENST00000325223.7:c.200T>G ENSP00000317302.7:p.Leu67Arg
ENST00000339818.8:c.200T>G ENSP00000344566.4:p.Leu67Arg
ENST00000397956.7:c.200T>G ENSP00000381047.3:p.Leu67Arg
ENST00000462742.1:n.2371T>G
ENST00000478674.1:n.259T>G
ENST00000496321.5:n.316T>G
NM_001271440.1:c.200T>G NP_001258369.1:p.Leu67Arg
NM_001271441.1:c.200T>G NP_001258370.1:p.Leu67Arg
NM_001271442.1:c.77T>G NP_001258371.1:p.Leu26Arg
NM_004928.2:c.200T>G NP_004919.1:p.Leu67Arg
XM_006724051.2:c.275T>G XP_006724114.1:p.Leu92Arg
XM_006724052.2:c.275T>G XP_006724115.1:p.Leu92Arg
XM_006724053.2:c.-125T>G XP_006724116.1:n.-125T>G
XR_937571.1:n.403T>G
XM_006724051.3:c.275T>G XP_006724114.1:p.Leu92Arg
XM_006724053.3:c.-125T>G XP_006724116.1:n.-125T>G
XM_017028470.1:c.404T>G XP_016883959.1:p.Leu135Arg
XM_017028471.1:c.149T>G XP_016883960.1:p.Leu50Arg
XM_017028472.1:c.-125T>G XP_016883961.1:n.-125T>G
XR_937571.2:n.410T>G
NM_004928.3:c.200T>G MANE Select NP_004919.1:p.Leu67Arg
NM_001271440.2:c.200T>G NP_001258369.1:p.Leu67Arg
NM_001271441.2:c.200T>G NP_001258370.1:p.Leu67Arg