Canonical Allele Identifier: CA2391590931

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333075C= , CM000683.2:g.44333075C=	GRCh38
NC_000021.8:g.45752958C= , CM000683.1:g.45752958C=	GRCh37
NC_000021.7:g.44577386C=	NCBI36
NG_032952.1:g.11328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.331G= MANE Select	ENSP00000344566.4:p.Val111=
ENST00000325223.7:c.331G=	ENSP00000317302.7:p.Val111=
ENST00000339818.8:c.331G=	ENSP00000344566.4:p.Val111=
ENST00000397956.7:c.331G=	ENSP00000381047.3:p.Val111=
ENST00000462742.1:n.2502G=
ENST00000478674.1:n.390G=
ENST00000496321.5:n.447G=
NM_001271440.1:c.331G=	NP_001258369.1:p.Val111=
NM_001271441.1:c.331G=	NP_001258370.1:p.Val111=
NM_001271442.1:c.208G=	NP_001258371.1:p.Val70=
NM_004928.2:c.331G=	NP_004919.1:p.Val111=
XM_006724051.2:c.406G=	XP_006724114.1:p.Val136=
XM_006724052.2:c.406G=	XP_006724115.1:p.Val136=
XM_006724053.2:c.7G=	XP_006724116.1:p.Val3=
XR_937571.1:n.534G=
XM_006724051.3:c.406G=	XP_006724114.1:p.Val136=
XM_006724053.3:c.7G=	XP_006724116.1:p.Val3=
XM_017028470.1:c.535G=	XP_016883959.1:p.Val179=
XM_017028471.1:c.280G=	XP_016883960.1:p.Val94=
XM_017028472.1:c.7G=	XP_016883961.1:p.Val3=
XR_937571.2:n.541G=
NM_004928.3:c.331G= MANE Select	NP_004919.1:p.Val111=
NM_001271440.2:c.331G=	NP_001258369.1:p.Val111=
NM_001271441.2:c.331G=	NP_001258370.1:p.Val111=