Canonical Allele Identifier: CA2391591030

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333248G= , CM000683.2:g.44333248G=	GRCh38
NC_000021.8:g.45753131G= , CM000683.1:g.45753131G=	GRCh37
NC_000021.7:g.44577559G=	NCBI36
NG_032952.1:g.11155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.158C= MANE Select	ENSP00000344566.4:p.Ser53=
ENST00000325223.7:c.158C=	ENSP00000317302.7:p.Ser53=
ENST00000339818.8:c.158C=	ENSP00000344566.4:p.Ser53=
ENST00000397956.7:c.158C=	ENSP00000381047.3:p.Ser53=
ENST00000462742.1:n.2329C=
ENST00000478674.1:n.217C=
ENST00000496321.5:n.274C=
NM_001271440.1:c.158C=	NP_001258369.1:p.Ser53=
NM_001271441.1:c.158C=	NP_001258370.1:p.Ser53=
NM_001271442.1:c.35C=	NP_001258371.1:p.Ser12=
NM_004928.2:c.158C=	NP_004919.1:p.Ser53=
XM_006724051.2:c.233C=	XP_006724114.1:p.Ser78=
XM_006724052.2:c.233C=	XP_006724115.1:p.Ser78=
XM_006724053.2:c.-167C=	XP_006724116.1:n.-167C=
XR_937571.1:n.361C=
XM_006724051.3:c.233C=	XP_006724114.1:p.Ser78=
XM_006724053.3:c.-167C=	XP_006724116.1:n.-167C=
XM_017028470.1:c.362C=	XP_016883959.1:p.Ser121=
XM_017028471.1:c.107C=	XP_016883960.1:p.Ser36=
XM_017028472.1:c.-167C=	XP_016883961.1:n.-167C=
XR_937571.2:n.368C=
NM_004928.3:c.158C= MANE Select	NP_004919.1:p.Ser53=
NM_001271440.2:c.158C=	NP_001258369.1:p.Ser53=
NM_001271441.2:c.158C=	NP_001258370.1:p.Ser53=