Canonical Allele Identifier: CA2737710762

Gene: CFAP410

Linked Data

• dbSNP Id: rs2146069727

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333265_44333266insAGCGTGATCACCTCCAGGCTGGGCATCTC , CM000683.2:g.44333265_44333266insAGCGTGATCACCTCCAGGCTGGGCATCTC	GRCh38
NC_000021.8:g.45753148_45753149insAGCGTGATCACCTCCAGGCTGGGCATCTC , CM000683.1:g.45753148_45753149insAGCGTGATCACCTCCAGGCTGGGCATCTC	GRCh37
NC_000021.7:g.44577576_44577577insAGCGTGATCACCTCCAGGCTGGGCATCTC	NCBI36
NG_032952.1:g.11137_11138insGAGATGCCCAGCCTGGAGGTGATCACGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT MANE Select	ENSP00000344566.4:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACG...
ENST00000325223.7:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	ENSP00000317302.7:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACG...
ENST00000339818.8:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	ENSP00000344566.4:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACG...
ENST00000397956.7:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	ENSP00000381047.3:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACG...
ENST00000462742.1:n.2315-4_2315-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
ENST00000478674.1:n.199_200insGAGATGCCCAGCCTGGAGGTGATCACGCT
ENST00000496321.5:n.269-13_269-12insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_001271440.1:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_001258369.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_001271441.1:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_001258370.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_001271442.1:c.30-13_30-12insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_001258371.1:n.30-13_30-12insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_004928.2:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_004919.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_006724051.2:c.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_006724114.1:n.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_006724052.2:c.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_006724115.1:n.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_006724053.2:c.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_006724116.1:n.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGC...
XR_937571.1:n.347-4_347-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_006724051.3:c.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_006724114.1:n.219-4_219-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_006724053.3:c.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_006724116.1:n.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGC...
XM_017028470.1:c.348-4_348-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_016883959.1:n.348-4_348-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_017028471.1:c.93-4_93-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_016883960.1:n.93-4_93-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
XM_017028472.1:c.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	XP_016883961.1:n.-181-4_-181-3insGAGATGCCCAGCCTGGAGGTGATCACGC...
XR_937571.2:n.354-4_354-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_004928.3:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT MANE Select	NP_004919.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_001271440.2:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_001258369.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT
NM_001271441.2:c.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT	NP_001258370.1:n.144-4_144-3insGAGATGCCCAGCCTGGAGGTGATCACGCT