Canonical Allele Identifier: CA2818043331

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333331_44333332insAGA , CM000683.2:g.44333331_44333332insAGA	GRCh38
NC_000021.8:g.45753214_45753215insAGA , CM000683.1:g.45753214_45753215insAGA	GRCh37
NC_000021.7:g.44577642_44577643insAGA	NCBI36
NG_032952.1:g.11071_11072insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-70_144-69insTCT MANE Select	ENSP00000344566.4:n.144-70_144-69insTCT
ENST00000325223.7:c.144-70_144-69insTCT	ENSP00000317302.7:n.144-70_144-69insTCT
ENST00000339818.8:c.144-70_144-69insTCT	ENSP00000344566.4:n.144-70_144-69insTCT
ENST00000397956.7:c.144-70_144-69insTCT	ENSP00000381047.3:n.144-70_144-69insTCT
ENST00000462742.1:n.2315-70_2315-69insTCT
ENST00000478674.1:n.133_134insTCT
ENST00000496321.5:n.269-79_269-78insTCT
NM_001271440.1:c.144-70_144-69insTCT	NP_001258369.1:n.144-70_144-69insTCT
NM_001271441.1:c.144-70_144-69insTCT	NP_001258370.1:n.144-70_144-69insTCT
NM_001271442.1:c.30-79_30-78insTCT	NP_001258371.1:n.30-79_30-78insTCT
NM_004928.2:c.144-70_144-69insTCT	NP_004919.1:n.144-70_144-69insTCT
XM_006724051.2:c.219-70_219-69insTCT	XP_006724114.1:n.219-70_219-69insTCT
XM_006724052.2:c.219-70_219-69insTCT	XP_006724115.1:n.219-70_219-69insTCT
XM_006724053.2:c.-181-70_-181-69insTCT	XP_006724116.1:n.-181-70_-181-69insTCT
XR_937571.1:n.347-70_347-69insTCT
XM_006724051.3:c.219-70_219-69insTCT	XP_006724114.1:n.219-70_219-69insTCT
XM_006724053.3:c.-181-70_-181-69insTCT	XP_006724116.1:n.-181-70_-181-69insTCT
XM_017028470.1:c.348-70_348-69insTCT	XP_016883959.1:n.348-70_348-69insTCT
XM_017028471.1:c.93-70_93-69insTCT	XP_016883960.1:n.93-70_93-69insTCT
XM_017028472.1:c.-181-70_-181-69insTCT	XP_016883961.1:n.-181-70_-181-69insTCT
XR_937571.2:n.354-70_354-69insTCT
NM_004928.3:c.144-70_144-69insTCT MANE Select	NP_004919.1:n.144-70_144-69insTCT
NM_001271440.2:c.144-70_144-69insTCT	NP_001258369.1:n.144-70_144-69insTCT
NM_001271441.2:c.144-70_144-69insTCT	NP_001258370.1:n.144-70_144-69insTCT