Canonical Allele Identifier: CA2391590997

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333186T= , CM000683.2:g.44333186T=	GRCh38
NC_000021.8:g.45753069T= , CM000683.1:g.45753069T=	GRCh37
NC_000021.7:g.44577497T=	NCBI36
NG_032952.1:g.11217A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.220A= MANE Select	ENSP00000344566.4:p.Ile74=
ENST00000325223.7:c.220A=	ENSP00000317302.7:p.Ile74=
ENST00000339818.8:c.220A=	ENSP00000344566.4:p.Ile74=
ENST00000397956.7:c.220A=	ENSP00000381047.3:p.Ile74=
ENST00000462742.1:n.2391A=
ENST00000478674.1:n.279A=
ENST00000496321.5:n.336A=
NM_001271440.1:c.220A=	NP_001258369.1:p.Ile74=
NM_001271441.1:c.220A=	NP_001258370.1:p.Ile74=
NM_001271442.1:c.97A=	NP_001258371.1:p.Ile33=
NM_004928.2:c.220A=	NP_004919.1:p.Ile74=
XM_006724051.2:c.295A=	XP_006724114.1:p.Ile99=
XM_006724052.2:c.295A=	XP_006724115.1:p.Ile99=
XM_006724053.2:c.-105A=	XP_006724116.1:n.-105A=
XR_937571.1:n.423A=
XM_006724051.3:c.295A=	XP_006724114.1:p.Ile99=
XM_006724053.3:c.-105A=	XP_006724116.1:n.-105A=
XM_017028470.1:c.424A=	XP_016883959.1:p.Ile142=
XM_017028471.1:c.169A=	XP_016883960.1:p.Ile57=
XM_017028472.1:c.-105A=	XP_016883961.1:n.-105A=
XR_937571.2:n.430A=
NM_004928.3:c.220A= MANE Select	NP_004919.1:p.Ile74=
NM_001271440.2:c.220A=	NP_001258369.1:p.Ile74=
NM_001271441.2:c.220A=	NP_001258370.1:p.Ile74=