Canonical Allele Identifier: CA2391590913

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333051G= , CM000683.2:g.44333051G=	GRCh38
NC_000021.8:g.45752934G= , CM000683.1:g.45752934G=	GRCh37
NC_000021.7:g.44577362G=	NCBI36
NG_032952.1:g.11352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.355C= MANE Select	ENSP00000344566.4:p.Gln119=
ENST00000325223.7:c.355C=	ENSP00000317302.7:p.Gln119=
ENST00000339818.8:c.355C=	ENSP00000344566.4:p.Gln119=
ENST00000397956.7:c.355C=	ENSP00000381047.3:p.Gln119=
ENST00000462742.1:n.2526C=
ENST00000478674.1:n.414C=
ENST00000496321.5:n.471C=
NM_001271440.1:c.355C=	NP_001258369.1:p.Gln119=
NM_001271441.1:c.355C=	NP_001258370.1:p.Gln119=
NM_001271442.1:c.232C=	NP_001258371.1:p.Gln78=
NM_004928.2:c.355C=	NP_004919.1:p.Gln119=
XM_006724051.2:c.430C=	XP_006724114.1:p.Gln144=
XM_006724052.2:c.430C=	XP_006724115.1:p.Gln144=
XM_006724053.2:c.31C=	XP_006724116.1:p.Gln11=
XR_937571.1:n.558C=
XM_006724051.3:c.430C=	XP_006724114.1:p.Gln144=
XM_006724053.3:c.31C=	XP_006724116.1:p.Gln11=
XM_017028470.1:c.559C=	XP_016883959.1:p.Gln187=
XM_017028471.1:c.304C=	XP_016883960.1:p.Gln102=
XM_017028472.1:c.31C=	XP_016883961.1:p.Gln11=
XR_937571.2:n.565C=
NM_004928.3:c.355C= MANE Select	NP_004919.1:p.Gln119=
NM_001271440.2:c.355C=	NP_001258369.1:p.Gln119=
NM_001271441.2:c.355C=	NP_001258370.1:p.Gln119=