Canonical Allele Identifier: CA2818043310

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333269_44333272del , CM000683.2:g.44333269_44333272del	GRCh38
NC_000021.8:g.45753152_45753155del , CM000683.1:g.45753152_45753155del	GRCh37
NC_000021.7:g.44577580_44577583del	NCBI36
NG_032952.1:g.11131_11134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-10_144-7del MANE Select	ENSP00000344566.4:n.144-10_144-7del
ENST00000325223.7:c.144-10_144-7del	ENSP00000317302.7:n.144-10_144-7del
ENST00000339818.8:c.144-10_144-7del	ENSP00000344566.4:n.144-10_144-7del
ENST00000397956.7:c.144-10_144-7del	ENSP00000381047.3:n.144-10_144-7del
ENST00000462742.1:n.2315-10_2315-7del
ENST00000478674.1:n.193_196del
ENST00000496321.5:n.269-19_269-16del
NM_001271440.1:c.144-10_144-7del	NP_001258369.1:n.144-10_144-7del
NM_001271441.1:c.144-10_144-7del	NP_001258370.1:n.144-10_144-7del
NM_001271442.1:c.30-19_30-16del	NP_001258371.1:n.30-19_30-16del
NM_004928.2:c.144-10_144-7del	NP_004919.1:n.144-10_144-7del
XM_006724051.2:c.219-10_219-7del	XP_006724114.1:n.219-10_219-7del
XM_006724052.2:c.219-10_219-7del	XP_006724115.1:n.219-10_219-7del
XM_006724053.2:c.-181-10_-181-7del	XP_006724116.1:n.-181-10_-181-7del
XR_937571.1:n.347-10_347-7del
XM_006724051.3:c.219-10_219-7del	XP_006724114.1:n.219-10_219-7del
XM_006724053.3:c.-181-10_-181-7del	XP_006724116.1:n.-181-10_-181-7del
XM_017028470.1:c.348-10_348-7del	XP_016883959.1:n.348-10_348-7del
XM_017028471.1:c.93-10_93-7del	XP_016883960.1:n.93-10_93-7del
XM_017028472.1:c.-181-10_-181-7del	XP_016883961.1:n.-181-10_-181-7del
XR_937571.2:n.354-10_354-7del
NM_004928.3:c.144-10_144-7del MANE Select	NP_004919.1:n.144-10_144-7del
NM_001271440.2:c.144-10_144-7del	NP_001258369.1:n.144-10_144-7del
NM_001271441.2:c.144-10_144-7del	NP_001258370.1:n.144-10_144-7del