Canonical Allele Identifier: CA2818043323

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333311_44333312insACA , CM000683.2:g.44333311_44333312insACA	GRCh38
NC_000021.8:g.45753194_45753195insACA , CM000683.1:g.45753194_45753195insACA	GRCh37
NC_000021.7:g.44577622_44577623insACA	NCBI36
NG_032952.1:g.11091_11092insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-50_144-49insTGT MANE Select	ENSP00000344566.4:n.144-50_144-49insTGT
ENST00000325223.7:c.144-50_144-49insTGT	ENSP00000317302.7:n.144-50_144-49insTGT
ENST00000339818.8:c.144-50_144-49insTGT	ENSP00000344566.4:n.144-50_144-49insTGT
ENST00000397956.7:c.144-50_144-49insTGT	ENSP00000381047.3:n.144-50_144-49insTGT
ENST00000462742.1:n.2315-50_2315-49insTGT
ENST00000478674.1:n.153_154insTGT
ENST00000496321.5:n.269-59_269-58insTGT
NM_001271440.1:c.144-50_144-49insTGT	NP_001258369.1:n.144-50_144-49insTGT
NM_001271441.1:c.144-50_144-49insTGT	NP_001258370.1:n.144-50_144-49insTGT
NM_001271442.1:c.30-59_30-58insTGT	NP_001258371.1:n.30-59_30-58insTGT
NM_004928.2:c.144-50_144-49insTGT	NP_004919.1:n.144-50_144-49insTGT
XM_006724051.2:c.219-50_219-49insTGT	XP_006724114.1:n.219-50_219-49insTGT
XM_006724052.2:c.219-50_219-49insTGT	XP_006724115.1:n.219-50_219-49insTGT
XM_006724053.2:c.-181-50_-181-49insTGT	XP_006724116.1:n.-181-50_-181-49insTGT
XR_937571.1:n.347-50_347-49insTGT
XM_006724051.3:c.219-50_219-49insTGT	XP_006724114.1:n.219-50_219-49insTGT
XM_006724053.3:c.-181-50_-181-49insTGT	XP_006724116.1:n.-181-50_-181-49insTGT
XM_017028470.1:c.348-50_348-49insTGT	XP_016883959.1:n.348-50_348-49insTGT
XM_017028471.1:c.93-50_93-49insTGT	XP_016883960.1:n.93-50_93-49insTGT
XM_017028472.1:c.-181-50_-181-49insTGT	XP_016883961.1:n.-181-50_-181-49insTGT
XR_937571.2:n.354-50_354-49insTGT
NM_004928.3:c.144-50_144-49insTGT MANE Select	NP_004919.1:n.144-50_144-49insTGT
NM_001271440.2:c.144-50_144-49insTGT	NP_001258369.1:n.144-50_144-49insTGT
NM_001271441.2:c.144-50_144-49insTGT	NP_001258370.1:n.144-50_144-49insTGT