Canonical Allele Identifier: CA2391589536

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44330298A= , CM000683.2:g.44330298A=	GRCh38
NC_000021.8:g.45750181A= , CM000683.1:g.45750181A=	GRCh37
NC_000021.7:g.44574609A=	NCBI36
NG_032952.1:g.14105T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.671T= MANE Select	ENSP00000344566.4:p.Leu224=
ENST00000325223.7:c.668T=	ENSP00000317302.7:p.Leu223=
ENST00000339818.8:c.671T=	ENSP00000344566.4:p.Leu224=
ENST00000397956.7:c.1028T=	ENSP00000381047.3:p.Leu343=
ENST00000462742.1:n.4125T=
ENST00000470196.5:n.247T=
ENST00000496321.5:n.784T=
NM_001271440.1:c.668T=	NP_001258369.1:p.Leu223=
NM_001271441.1:c.1028T=	NP_001258370.1:p.Leu343=
NM_001271442.1:c.545T=	NP_001258371.1:p.Leu182=
NM_004928.2:c.671T=	NP_004919.1:p.Leu224=
XM_006724051.2:c.746T=	XP_006724114.1:p.Leu249=
XM_006724052.2:c.743T=	XP_006724115.1:p.Leu248=
XM_006724053.2:c.347T=	XP_006724116.1:p.Leu116=
XR_937571.1:n.1231T=
XM_006724051.3:c.746T=	XP_006724114.1:p.Leu249=
XM_006724053.3:c.347T=	XP_006724116.1:p.Leu116=
XM_017028470.1:c.872T=	XP_016883959.1:p.Leu291=
XM_017028471.1:c.620T=	XP_016883960.1:p.Leu207=
XM_017028472.1:c.344T=	XP_016883961.1:p.Leu115=
XR_937571.2:n.1238T=
NM_004928.3:c.671T= MANE Select	NP_004919.1:p.Leu224=
NM_001271440.2:c.668T=	NP_001258369.1:p.Leu223=
NM_001271441.2:c.1028T=	NP_001258370.1:p.Leu343=