Canonical Allele Identifier: CA410456374
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333087A>T , CM000683.2:g.44333087A>T GRCh38
NC_000021.8:g.45752970A>T , CM000683.1:g.45752970A>T GRCh37
NC_000021.7:g.44577398A>T NCBI36
NG_032952.1:g.11316T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.319T>A MANE Select ENSP00000344566.4:p.Tyr107Asn
ENST00000325223.7:c.319T>A ENSP00000317302.7:p.Tyr107Asn
ENST00000339818.8:c.319T>A ENSP00000344566.4:p.Tyr107Asn
ENST00000397956.7:c.319T>A ENSP00000381047.3:p.Tyr107Asn
ENST00000462742.1:n.2490T>A
ENST00000478674.1:n.378T>A
ENST00000496321.5:n.435T>A
NM_001271440.1:c.319T>A NP_001258369.1:p.Tyr107Asn
NM_001271441.1:c.319T>A NP_001258370.1:p.Tyr107Asn
NM_001271442.1:c.196T>A NP_001258371.1:p.Tyr66Asn
NM_004928.2:c.319T>A NP_004919.1:p.Tyr107Asn
XM_006724051.2:c.394T>A XP_006724114.1:p.Tyr132Asn
XM_006724052.2:c.394T>A XP_006724115.1:p.Tyr132Asn
XM_006724053.2:c.-6T>A XP_006724116.1:n.-6T>A
XR_937571.1:n.522T>A
XM_006724051.3:c.394T>A XP_006724114.1:p.Tyr132Asn
XM_006724053.3:c.-6T>A XP_006724116.1:n.-6T>A
XM_017028470.1:c.523T>A XP_016883959.1:p.Tyr175Asn
XM_017028471.1:c.268T>A XP_016883960.1:p.Tyr90Asn
XM_017028472.1:c.-6T>A XP_016883961.1:n.-6T>A
XR_937571.2:n.529T>A
NM_004928.3:c.319T>A MANE Select NP_004919.1:p.Tyr107Asn
NM_001271440.2:c.319T>A NP_001258369.1:p.Tyr107Asn
NM_001271441.2:c.319T>A NP_001258370.1:p.Tyr107Asn