Canonical Allele Identifier: CA2391591016

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333226C= , CM000683.2:g.44333226C=	GRCh38
NC_000021.8:g.45753109C= , CM000683.1:g.45753109C=	GRCh37
NC_000021.7:g.44577537C=	NCBI36
NG_032952.1:g.11177G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000339818.9:c.180G= MANE Select	ENSP00000344566.4:p.Arg60=
ENST00000325223.7:c.180G=	ENSP00000317302.7:p.Arg60=
ENST00000339818.8:c.180G=	ENSP00000344566.4:p.Arg60=
ENST00000397956.7:c.180G=	ENSP00000381047.3:p.Arg60=
ENST00000462742.1:n.2351G=
ENST00000478674.1:n.239G=
ENST00000496321.5:n.296G=
NM_001271440.1:c.180G=	NP_001258369.1:p.Arg60=
NM_001271441.1:c.180G=	NP_001258370.1:p.Arg60=
NM_001271442.1:c.57G=	NP_001258371.1:p.Arg19=
NM_004928.2:c.180G=	NP_004919.1:p.Arg60=
XM_006724051.2:c.255G=	XP_006724114.1:p.Arg85=
XM_006724052.2:c.255G=	XP_006724115.1:p.Arg85=
XM_006724053.2:c.-145G=	XP_006724116.1:n.-145G=
XR_937571.1:n.383G=
XM_006724051.3:c.255G=	XP_006724114.1:p.Arg85=
XM_006724053.3:c.-145G=	XP_006724116.1:n.-145G=
XM_017028470.1:c.384G=	XP_016883959.1:p.Arg128=
XM_017028471.1:c.129G=	XP_016883960.1:p.Arg43=
XM_017028472.1:c.-145G=	XP_016883961.1:n.-145G=
XR_937571.2:n.390G=
NM_004928.3:c.180G= MANE Select	NP_004919.1:p.Arg60=
NM_001271440.2:c.180G=	NP_001258369.1:p.Arg60=
NM_001271441.2:c.180G=	NP_001258370.1:p.Arg60=