Canonical Allele Identifier: CA2818043334

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333336_44333337insAG , CM000683.2:g.44333336_44333337insAG	GRCh38
NC_000021.8:g.45753219_45753220insAG , CM000683.1:g.45753219_45753220insAG	GRCh37
NC_000021.7:g.44577647_44577648insAG	NCBI36
NG_032952.1:g.11066_11067insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-75_144-74insCT MANE Select	ENSP00000344566.4:n.144-75_144-74insCT
ENST00000325223.7:c.144-75_144-74insCT	ENSP00000317302.7:n.144-75_144-74insCT
ENST00000339818.8:c.144-75_144-74insCT	ENSP00000344566.4:n.144-75_144-74insCT
ENST00000397956.7:c.144-75_144-74insCT	ENSP00000381047.3:n.144-75_144-74insCT
ENST00000462742.1:n.2315-75_2315-74insCT
ENST00000478674.1:n.128_129insCT
ENST00000496321.5:n.269-84_269-83insCT
NM_001271440.1:c.144-75_144-74insCT	NP_001258369.1:n.144-75_144-74insCT
NM_001271441.1:c.144-75_144-74insCT	NP_001258370.1:n.144-75_144-74insCT
NM_001271442.1:c.30-84_30-83insCT	NP_001258371.1:n.30-84_30-83insCT
NM_004928.2:c.144-75_144-74insCT	NP_004919.1:n.144-75_144-74insCT
XM_006724051.2:c.219-75_219-74insCT	XP_006724114.1:n.219-75_219-74insCT
XM_006724052.2:c.219-75_219-74insCT	XP_006724115.1:n.219-75_219-74insCT
XM_006724053.2:c.-181-75_-181-74insCT	XP_006724116.1:n.-181-75_-181-74insCT
XR_937571.1:n.347-75_347-74insCT
XM_006724051.3:c.219-75_219-74insCT	XP_006724114.1:n.219-75_219-74insCT
XM_006724053.3:c.-181-75_-181-74insCT	XP_006724116.1:n.-181-75_-181-74insCT
XM_017028470.1:c.348-75_348-74insCT	XP_016883959.1:n.348-75_348-74insCT
XM_017028471.1:c.93-75_93-74insCT	XP_016883960.1:n.93-75_93-74insCT
XM_017028472.1:c.-181-75_-181-74insCT	XP_016883961.1:n.-181-75_-181-74insCT
XR_937571.2:n.354-75_354-74insCT
NM_004928.3:c.144-75_144-74insCT MANE Select	NP_004919.1:n.144-75_144-74insCT
NM_001271440.2:c.144-75_144-74insCT	NP_001258369.1:n.144-75_144-74insCT
NM_001271441.2:c.144-75_144-74insCT	NP_001258370.1:n.144-75_144-74insCT