Canonical Allele Identifier: CA410456474
Gene: CFAP410 HGNC NCBI

Linked Data

dbSNP Id: rs2047682363

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333104C>T , CM000683.2:g.44333104C>T GRCh38
NC_000021.8:g.45752987C>T , CM000683.1:g.45752987C>T GRCh37
NC_000021.7:g.44577415C>T NCBI36
NG_032952.1:g.11299G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.302G>A MANE Select ENSP00000344566.4:p.Gly101Asp
ENST00000325223.7:c.302G>A ENSP00000317302.7:p.Gly101Asp
ENST00000339818.8:c.302G>A ENSP00000344566.4:p.Gly101Asp
ENST00000397956.7:c.302G>A ENSP00000381047.3:p.Gly101Asp
ENST00000462742.1:n.2473G>A
ENST00000478674.1:n.361G>A
ENST00000496321.5:n.418G>A
NM_001271440.1:c.302G>A NP_001258369.1:p.Gly101Asp
NM_001271441.1:c.302G>A NP_001258370.1:p.Gly101Asp
NM_001271442.1:c.179G>A NP_001258371.1:p.Gly60Asp
NM_004928.2:c.302G>A NP_004919.1:p.Gly101Asp
XM_006724051.2:c.377G>A XP_006724114.1:p.Gly126Asp
XM_006724052.2:c.377G>A XP_006724115.1:p.Gly126Asp
XM_006724053.2:c.-23G>A XP_006724116.1:n.-23G>A
XR_937571.1:n.505G>A
XM_006724051.3:c.377G>A XP_006724114.1:p.Gly126Asp
XM_006724053.3:c.-23G>A XP_006724116.1:n.-23G>A
XM_017028470.1:c.506G>A XP_016883959.1:p.Gly169Asp
XM_017028471.1:c.251G>A XP_016883960.1:p.Gly84Asp
XM_017028472.1:c.-23G>A XP_016883961.1:n.-23G>A
XR_937571.2:n.512G>A
NM_004928.3:c.302G>A MANE Select NP_004919.1:p.Gly101Asp
NM_001271440.2:c.302G>A NP_001258369.1:p.Gly101Asp
NM_001271441.2:c.302G>A NP_001258370.1:p.Gly101Asp