Canonical Allele Identifier: CA2818043324

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333312_44333313insAGA , CM000683.2:g.44333312_44333313insAGA	GRCh38
NC_000021.8:g.45753195_45753196insAGA , CM000683.1:g.45753195_45753196insAGA	GRCh37
NC_000021.7:g.44577623_44577624insAGA	NCBI36
NG_032952.1:g.11090_11091insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-51_144-50insTCT MANE Select	ENSP00000344566.4:n.144-51_144-50insTCT
ENST00000325223.7:c.144-51_144-50insTCT	ENSP00000317302.7:n.144-51_144-50insTCT
ENST00000339818.8:c.144-51_144-50insTCT	ENSP00000344566.4:n.144-51_144-50insTCT
ENST00000397956.7:c.144-51_144-50insTCT	ENSP00000381047.3:n.144-51_144-50insTCT
ENST00000462742.1:n.2315-51_2315-50insTCT
ENST00000478674.1:n.152_153insTCT
ENST00000496321.5:n.269-60_269-59insTCT
NM_001271440.1:c.144-51_144-50insTCT	NP_001258369.1:n.144-51_144-50insTCT
NM_001271441.1:c.144-51_144-50insTCT	NP_001258370.1:n.144-51_144-50insTCT
NM_001271442.1:c.30-60_30-59insTCT	NP_001258371.1:n.30-60_30-59insTCT
NM_004928.2:c.144-51_144-50insTCT	NP_004919.1:n.144-51_144-50insTCT
XM_006724051.2:c.219-51_219-50insTCT	XP_006724114.1:n.219-51_219-50insTCT
XM_006724052.2:c.219-51_219-50insTCT	XP_006724115.1:n.219-51_219-50insTCT
XM_006724053.2:c.-181-51_-181-50insTCT	XP_006724116.1:n.-181-51_-181-50insTCT
XR_937571.1:n.347-51_347-50insTCT
XM_006724051.3:c.219-51_219-50insTCT	XP_006724114.1:n.219-51_219-50insTCT
XM_006724053.3:c.-181-51_-181-50insTCT	XP_006724116.1:n.-181-51_-181-50insTCT
XM_017028470.1:c.348-51_348-50insTCT	XP_016883959.1:n.348-51_348-50insTCT
XM_017028471.1:c.93-51_93-50insTCT	XP_016883960.1:n.93-51_93-50insTCT
XM_017028472.1:c.-181-51_-181-50insTCT	XP_016883961.1:n.-181-51_-181-50insTCT
XR_937571.2:n.354-51_354-50insTCT
NM_004928.3:c.144-51_144-50insTCT MANE Select	NP_004919.1:n.144-51_144-50insTCT
NM_001271440.2:c.144-51_144-50insTCT	NP_001258369.1:n.144-51_144-50insTCT
NM_001271441.2:c.144-51_144-50insTCT	NP_001258370.1:n.144-51_144-50insTCT