Canonical Allele Identifier: CA2695230204

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333054_44333055insCGCGGCAGGGTG , CM000683.2:g.44333054_44333055insCGCGGCAGGGTG	GRCh38
NC_000021.8:g.45752937_45752938insCGCGGCAGGGTG , CM000683.1:g.45752937_45752938insCGCGGCAGGGTG	GRCh37
NC_000021.7:g.44577365_44577366insCGCGGCAGGGTG	NCBI36
NG_032952.1:g.11349_11350insACCCTGCCGCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.352_353insACCCTGCCGCGC MANE Select	ENSP00000344566.4:p.Arg117_Leu118insHisProAlaAla
ENST00000325223.7:c.352_353insACCCTGCCGCGC	ENSP00000317302.7:p.Arg117_Leu118insHisProAlaAla
ENST00000339818.8:c.352_353insACCCTGCCGCGC	ENSP00000344566.4:p.Arg117_Leu118insHisProAlaAla
ENST00000397956.7:c.352_353insACCCTGCCGCGC	ENSP00000381047.3:p.Arg117_Leu118insHisProAlaAla
ENST00000462742.1:n.2523_2524insACCCTGCCGCGC
ENST00000478674.1:n.411_412insACCCTGCCGCGC
ENST00000496321.5:n.468_469insACCCTGCCGCGC
NM_001271440.1:c.352_353insACCCTGCCGCGC	NP_001258369.1:p.Arg117_Leu118insHisProAlaAla
NM_001271441.1:c.352_353insACCCTGCCGCGC	NP_001258370.1:p.Arg117_Leu118insHisProAlaAla
NM_001271442.1:c.229_230insACCCTGCCGCGC	NP_001258371.1:p.Arg76_Leu77insHisProAlaAla
NM_004928.2:c.352_353insACCCTGCCGCGC	NP_004919.1:p.Arg117_Leu118insHisProAlaAla
XM_006724051.2:c.427_428insACCCTGCCGCGC	XP_006724114.1:p.Arg142_Leu143insHisProAlaAla
XM_006724052.2:c.427_428insACCCTGCCGCGC	XP_006724115.1:p.Arg142_Leu143insHisProAlaAla
XM_006724053.2:c.28_29insACCCTGCCGCGC	XP_006724116.1:p.Arg9_Leu10insHisProAlaAla
XR_937571.1:n.555_556insACCCTGCCGCGC
XM_006724051.3:c.427_428insACCCTGCCGCGC	XP_006724114.1:p.Arg142_Leu143insHisProAlaAla
XM_006724053.3:c.28_29insACCCTGCCGCGC	XP_006724116.1:p.Arg9_Leu10insHisProAlaAla
XM_017028470.1:c.556_557insACCCTGCCGCGC	XP_016883959.1:p.Arg185_Leu186insHisProAlaAla
XM_017028471.1:c.301_302insACCCTGCCGCGC	XP_016883960.1:p.Arg100_Leu101insHisProAlaAla
XM_017028472.1:c.28_29insACCCTGCCGCGC	XP_016883961.1:p.Arg9_Leu10insHisProAlaAla
XR_937571.2:n.562_563insACCCTGCCGCGC
NM_004928.3:c.352_353insACCCTGCCGCGC MANE Select	NP_004919.1:p.Arg117_Leu118insHisProAlaAla
NM_001271440.2:c.352_353insACCCTGCCGCGC	NP_001258369.1:p.Arg117_Leu118insHisProAlaAla
NM_001271441.2:c.352_353insACCCTGCCGCGC	NP_001258370.1:p.Arg117_Leu118insHisProAlaAla