Canonical Allele Identifier: CA410456942
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333153C>G , CM000683.2:g.44333153C>G GRCh38
NC_000021.8:g.45753036C>G , CM000683.1:g.45753036C>G GRCh37
NC_000021.7:g.44577464C>G NCBI36
NG_032952.1:g.11250G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.253G>C MANE Select ENSP00000344566.4:p.Gly85Arg
ENST00000325223.7:c.253G>C ENSP00000317302.7:p.Gly85Arg
ENST00000339818.8:c.253G>C ENSP00000344566.4:p.Gly85Arg
ENST00000397956.7:c.253G>C ENSP00000381047.3:p.Gly85Arg
ENST00000462742.1:n.2424G>C
ENST00000478674.1:n.312G>C
ENST00000496321.5:n.369G>C
NM_001271440.1:c.253G>C NP_001258369.1:p.Gly85Arg
NM_001271441.1:c.253G>C NP_001258370.1:p.Gly85Arg
NM_001271442.1:c.130G>C NP_001258371.1:p.Gly44Arg
NM_004928.2:c.253G>C NP_004919.1:p.Gly85Arg
XM_006724051.2:c.328G>C XP_006724114.1:p.Gly110Arg
XM_006724052.2:c.328G>C XP_006724115.1:p.Gly110Arg
XM_006724053.2:c.-72G>C XP_006724116.1:n.-72G>C
XR_937571.1:n.456G>C
XM_006724051.3:c.328G>C XP_006724114.1:p.Gly110Arg
XM_006724053.3:c.-72G>C XP_006724116.1:n.-72G>C
XM_017028470.1:c.457G>C XP_016883959.1:p.Gly153Arg
XM_017028471.1:c.202G>C XP_016883960.1:p.Gly68Arg
XM_017028472.1:c.-72G>C XP_016883961.1:n.-72G>C
XR_937571.2:n.463G>C
NM_004928.3:c.253G>C MANE Select NP_004919.1:p.Gly85Arg
NM_001271440.2:c.253G>C NP_001258369.1:p.Gly85Arg
NM_001271441.2:c.253G>C NP_001258370.1:p.Gly85Arg