Canonical Allele Identifier: CA2391592223

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44335798T= , CM000683.2:g.44335798T=	GRCh38
NC_000021.8:g.45755681T= , CM000683.1:g.45755681T=	GRCh37
NC_000021.7:g.44580109T=	NCBI36
NG_032952.1:g.8605A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004928.3:c.103A= MANE Select	NP_004919.1:p.Ile35=
ENST00000339818.9:c.103A= MANE Select	ENSP00000344566.4:p.Ile35=
NM_001271440.1:c.103A=	NP_001258369.1:p.Ile35=
NM_001271440.2:c.103A=	NP_001258369.1:p.Ile35=
NM_001271441.1:c.103A=	NP_001258370.1:p.Ile35=
NM_001271441.2:c.103A=	NP_001258370.1:p.Ile35=
NM_001271442.1:c.-12A=	NP_001258371.1:n.-12A=
NM_004928.2:c.103A=	NP_004919.1:p.Ile35=
ENST00000325223.7:c.103A=	ENSP00000317302.7:p.Ile35=
ENST00000339818.8:c.103A=	ENSP00000344566.4:p.Ile35=
ENST00000397956.7:c.103A=	ENSP00000381047.3:p.Ile35=
ENST00000462742.1:n.577A=
ENST00000496321.5:n.228A=
XM_006724051.2:c.218+1851A=	XP_006724114.1:n.218+1851A=
XM_006724051.3:c.218+1851A=	XP_006724114.1:n.218+1851A=
XM_006724052.2:c.218+1851A=	XP_006724115.1:n.218+1851A=
XM_006724053.2:c.-182+1851A=	XP_006724116.1:n.-182+1851A=
XM_006724053.3:c.-182+1851A=	XP_006724116.1:n.-182+1851A=
XM_017028470.1:c.307A=	XP_016883959.1:p.Ile103=
XM_017028471.1:c.92+1851A=	XP_016883960.1:n.92+1851A=
XM_017028472.1:c.-182+1851A=	XP_016883961.1:n.-182+1851A=
XR_937571.1:n.306A=
XR_937571.2:n.313A=