Canonical Allele Identifier: CA2391591012

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333220C= , CM000683.2:g.44333220C=	GRCh38
NC_000021.8:g.45753103C= , CM000683.1:g.45753103C=	GRCh37
NC_000021.7:g.44577531C=	NCBI36
NG_032952.1:g.11183G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.186G= MANE Select	ENSP00000344566.4:p.Gln62=
ENST00000325223.7:c.186G=	ENSP00000317302.7:p.Gln62=
ENST00000339818.8:c.186G=	ENSP00000344566.4:p.Gln62=
ENST00000397956.7:c.186G=	ENSP00000381047.3:p.Gln62=
ENST00000462742.1:n.2357G=
ENST00000478674.1:n.245G=
ENST00000496321.5:n.302G=
NM_001271440.1:c.186G=	NP_001258369.1:p.Gln62=
NM_001271441.1:c.186G=	NP_001258370.1:p.Gln62=
NM_001271442.1:c.63G=	NP_001258371.1:p.Gln21=
NM_004928.2:c.186G=	NP_004919.1:p.Gln62=
XM_006724051.2:c.261G=	XP_006724114.1:p.Gln87=
XM_006724052.2:c.261G=	XP_006724115.1:p.Gln87=
XM_006724053.2:c.-139G=	XP_006724116.1:n.-139G=
XR_937571.1:n.389G=
XM_006724051.3:c.261G=	XP_006724114.1:p.Gln87=
XM_006724053.3:c.-139G=	XP_006724116.1:n.-139G=
XM_017028470.1:c.390G=	XP_016883959.1:p.Gln130=
XM_017028471.1:c.135G=	XP_016883960.1:p.Gln45=
XM_017028472.1:c.-139G=	XP_016883961.1:n.-139G=
XR_937571.2:n.396G=
NM_004928.3:c.186G= MANE Select	NP_004919.1:p.Gln62=
NM_001271440.2:c.186G=	NP_001258369.1:p.Gln62=
NM_001271441.2:c.186G=	NP_001258370.1:p.Gln62=