Canonical Allele Identifier: CA2391590925

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333066T= , CM000683.2:g.44333066T=	GRCh38
NC_000021.8:g.45752949T= , CM000683.1:g.45752949T=	GRCh37
NC_000021.7:g.44577377T=	NCBI36
NG_032952.1:g.11337A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.340A= MANE Select	ENSP00000344566.4:p.Thr114=
ENST00000325223.7:c.340A=	ENSP00000317302.7:p.Thr114=
ENST00000339818.8:c.340A=	ENSP00000344566.4:p.Thr114=
ENST00000397956.7:c.340A=	ENSP00000381047.3:p.Thr114=
ENST00000462742.1:n.2511A=
ENST00000478674.1:n.399A=
ENST00000496321.5:n.456A=
NM_001271440.1:c.340A=	NP_001258369.1:p.Thr114=
NM_001271441.1:c.340A=	NP_001258370.1:p.Thr114=
NM_001271442.1:c.217A=	NP_001258371.1:p.Thr73=
NM_004928.2:c.340A=	NP_004919.1:p.Thr114=
XM_006724051.2:c.415A=	XP_006724114.1:p.Thr139=
XM_006724052.2:c.415A=	XP_006724115.1:p.Thr139=
XM_006724053.2:c.16A=	XP_006724116.1:p.Thr6=
XR_937571.1:n.543A=
XM_006724051.3:c.415A=	XP_006724114.1:p.Thr139=
XM_006724053.3:c.16A=	XP_006724116.1:p.Thr6=
XM_017028470.1:c.544A=	XP_016883959.1:p.Thr182=
XM_017028471.1:c.289A=	XP_016883960.1:p.Thr97=
XM_017028472.1:c.16A=	XP_016883961.1:p.Thr6=
XR_937571.2:n.550A=
NM_004928.3:c.340A= MANE Select	NP_004919.1:p.Thr114=
NM_001271440.2:c.340A=	NP_001258369.1:p.Thr114=
NM_001271441.2:c.340A=	NP_001258370.1:p.Thr114=