Canonical Allele Identifier: CA2391590984

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333158A= , CM000683.2:g.44333158A=	GRCh38
NC_000021.8:g.45753041A= , CM000683.1:g.45753041A=	GRCh37
NC_000021.7:g.44577469A=	NCBI36
NG_032952.1:g.11245T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.248T= MANE Select	ENSP00000344566.4:p.Leu83=
ENST00000325223.7:c.248T=	ENSP00000317302.7:p.Leu83=
ENST00000339818.8:c.248T=	ENSP00000344566.4:p.Leu83=
ENST00000397956.7:c.248T=	ENSP00000381047.3:p.Leu83=
ENST00000462742.1:n.2419T=
ENST00000478674.1:n.307T=
ENST00000496321.5:n.364T=
NM_001271440.1:c.248T=	NP_001258369.1:p.Leu83=
NM_001271441.1:c.248T=	NP_001258370.1:p.Leu83=
NM_001271442.1:c.125T=	NP_001258371.1:p.Leu42=
NM_004928.2:c.248T=	NP_004919.1:p.Leu83=
XM_006724051.2:c.323T=	XP_006724114.1:p.Leu108=
XM_006724052.2:c.323T=	XP_006724115.1:p.Leu108=
XM_006724053.2:c.-77T=	XP_006724116.1:n.-77T=
XR_937571.1:n.451T=
XM_006724051.3:c.323T=	XP_006724114.1:p.Leu108=
XM_006724053.3:c.-77T=	XP_006724116.1:n.-77T=
XM_017028470.1:c.452T=	XP_016883959.1:p.Leu151=
XM_017028471.1:c.197T=	XP_016883960.1:p.Leu66=
XM_017028472.1:c.-77T=	XP_016883961.1:n.-77T=
XR_937571.2:n.458T=
NM_004928.3:c.248T= MANE Select	NP_004919.1:p.Leu83=
NM_001271440.2:c.248T=	NP_001258369.1:p.Leu83=
NM_001271441.2:c.248T=	NP_001258370.1:p.Leu83=