Canonical Allele Identifier: CA2818043319

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333303_44333304insA , CM000683.2:g.44333303_44333304insA	GRCh38
NC_000021.8:g.45753186_45753187insA , CM000683.1:g.45753186_45753187insA	GRCh37
NC_000021.7:g.44577614_44577615insA	NCBI36
NG_032952.1:g.11099_11100insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-42_144-41insT MANE Select	ENSP00000344566.4:n.144-42_144-41insT
ENST00000325223.7:c.144-42_144-41insT	ENSP00000317302.7:n.144-42_144-41insT
ENST00000339818.8:c.144-42_144-41insT	ENSP00000344566.4:n.144-42_144-41insT
ENST00000397956.7:c.144-42_144-41insT	ENSP00000381047.3:n.144-42_144-41insT
ENST00000462742.1:n.2315-42_2315-41insT
ENST00000478674.1:n.161_162insT
ENST00000496321.5:n.269-51_269-50insT
NM_001271440.1:c.144-42_144-41insT	NP_001258369.1:n.144-42_144-41insT
NM_001271441.1:c.144-42_144-41insT	NP_001258370.1:n.144-42_144-41insT
NM_001271442.1:c.30-51_30-50insT	NP_001258371.1:n.30-51_30-50insT
NM_004928.2:c.144-42_144-41insT	NP_004919.1:n.144-42_144-41insT
XM_006724051.2:c.219-42_219-41insT	XP_006724114.1:n.219-42_219-41insT
XM_006724052.2:c.219-42_219-41insT	XP_006724115.1:n.219-42_219-41insT
XM_006724053.2:c.-181-42_-181-41insT	XP_006724116.1:n.-181-42_-181-41insT
XR_937571.1:n.347-42_347-41insT
XM_006724051.3:c.219-42_219-41insT	XP_006724114.1:n.219-42_219-41insT
XM_006724053.3:c.-181-42_-181-41insT	XP_006724116.1:n.-181-42_-181-41insT
XM_017028470.1:c.348-42_348-41insT	XP_016883959.1:n.348-42_348-41insT
XM_017028471.1:c.93-42_93-41insT	XP_016883960.1:n.93-42_93-41insT
XM_017028472.1:c.-181-42_-181-41insT	XP_016883961.1:n.-181-42_-181-41insT
XR_937571.2:n.354-42_354-41insT
NM_004928.3:c.144-42_144-41insT MANE Select	NP_004919.1:n.144-42_144-41insT
NM_001271440.2:c.144-42_144-41insT	NP_001258369.1:n.144-42_144-41insT
NM_001271441.2:c.144-42_144-41insT	NP_001258370.1:n.144-42_144-41insT