Canonical Allele Identifier: CA410457673
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333251A>T , CM000683.2:g.44333251A>T GRCh38
NC_000021.8:g.45753134A>T , CM000683.1:g.45753134A>T GRCh37
NC_000021.7:g.44577562A>T NCBI36
NG_032952.1:g.11152T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.155T>A MANE Select ENSP00000344566.4:p.Ile52Asn
ENST00000325223.7:c.155T>A ENSP00000317302.7:p.Ile52Asn
ENST00000339818.8:c.155T>A ENSP00000344566.4:p.Ile52Asn
ENST00000397956.7:c.155T>A ENSP00000381047.3:p.Ile52Asn
ENST00000462742.1:n.2326T>A
ENST00000478674.1:n.214T>A
ENST00000496321.5:n.271T>A
NM_001271440.1:c.155T>A NP_001258369.1:p.Ile52Asn
NM_001271441.1:c.155T>A NP_001258370.1:p.Ile52Asn
NM_001271442.1:c.32T>A NP_001258371.1:p.Ile11Asn
NM_004928.2:c.155T>A NP_004919.1:p.Ile52Asn
XM_006724051.2:c.230T>A XP_006724114.1:p.Ile77Asn
XM_006724052.2:c.230T>A XP_006724115.1:p.Ile77Asn
XM_006724053.2:c.-170T>A XP_006724116.1:n.-170T>A
XR_937571.1:n.358T>A
XM_006724051.3:c.230T>A XP_006724114.1:p.Ile77Asn
XM_006724053.3:c.-170T>A XP_006724116.1:n.-170T>A
XM_017028470.1:c.359T>A XP_016883959.1:p.Ile120Asn
XM_017028471.1:c.104T>A XP_016883960.1:p.Ile35Asn
XM_017028472.1:c.-170T>A XP_016883961.1:n.-170T>A
XR_937571.2:n.365T>A
NM_004928.3:c.155T>A MANE Select NP_004919.1:p.Ile52Asn
NM_001271440.2:c.155T>A NP_001258369.1:p.Ile52Asn
NM_001271441.2:c.155T>A NP_001258370.1:p.Ile52Asn