Canonical Allele Identifier: CA2391589538
Gene: CFAP410 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44330300C= , CM000683.2:g.44330300C= GRCh38
NC_000021.8:g.45750183C= , CM000683.1:g.45750183C= GRCh37
NC_000021.7:g.44574611C= NCBI36
NG_032952.1:g.14103G=

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.669G= MANE Select ENSP00000344566.4:p.Leu223=
ENST00000325223.7:c.666G= ENSP00000317302.7:p.Leu222=
ENST00000339818.8:c.669G= ENSP00000344566.4:p.Leu223=
ENST00000397956.7:c.1026G= ENSP00000381047.3:p.Leu342=
ENST00000462742.1:n.4123G=
ENST00000470196.5:n.245G=
ENST00000496321.5:n.782G=
NM_001271440.1:c.666G= NP_001258369.1:p.Leu222=
NM_001271441.1:c.1026G= NP_001258370.1:p.Leu342=
NM_001271442.1:c.543G= NP_001258371.1:p.Leu181=
NM_004928.2:c.669G= NP_004919.1:p.Leu223=
XM_006724051.2:c.744G= XP_006724114.1:p.Leu248=
XM_006724052.2:c.741G= XP_006724115.1:p.Leu247=
XM_006724053.2:c.345G= XP_006724116.1:p.Leu115=
XR_937571.1:n.1229G=
XM_006724051.3:c.744G= XP_006724114.1:p.Leu248=
XM_006724053.3:c.345G= XP_006724116.1:p.Leu115=
XM_017028470.1:c.870G= XP_016883959.1:p.Leu290=
XM_017028471.1:c.618G= XP_016883960.1:p.Leu206=
XM_017028472.1:c.342G= XP_016883961.1:p.Leu114=
XR_937571.2:n.1236G=
NM_004928.3:c.669G= MANE Select NP_004919.1:p.Leu223=
NM_001271440.2:c.666G= NP_001258369.1:p.Leu222=
NM_001271441.2:c.1026G= NP_001258370.1:p.Leu342=