Canonical Allele Identifier: CA9824134

Gene: NCOA6

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34757941_34757943del , CM000682.2:g.34757941_34757943del	GRCh38
NC_000020.10:g.33345744_33345746del , CM000682.1:g.33345744_33345746del	GRCh37
NC_000020.9:g.32809405_32809407del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014071.5:c.828_830del MANE Select	NP_054790.2:p.Gln277del
ENST00000359003.7:c.828_830del MANE Select	ENSP00000351894.2:p.Gln277del
NM_001242539.1:c.828_830del	NP_001229468.1:p.Gln277del
NM_001242539.2:c.828_830del	NP_001229468.1:p.Gln277del
NM_001318240.1:c.828_830del	NP_001305169.1:p.Gln277del
NM_014071.3:c.828_830del	NP_054790.2:p.Gln277del
NM_014071.4:c.828_830del	NP_054790.2:p.Gln277del
ENST00000359003.6:c.828_830del	ENSP00000351894.2:p.Gln277del
ENST00000374796.6:c.828_830del	ENSP00000363929.2:p.Gln277del
ENST00000612493.4:c.828_830del	ENSP00000481177.1:p.Gln277del
ENST00000616167.1:c.828_830del	ENSP00000481935.1:p.Gln277del
XM_006723755.2:c.828_830del	XP_006723818.1:p.Gln277del
XM_006723755.3:c.828_830del	XP_006723818.1:p.Gln277del
XM_011528721.1:c.843_845del	XP_011527023.1:p.Gln282del
XM_011528721.3:c.843_845del	XP_011527023.1:p.Gln282del
XM_011528722.1:c.843_845del	XP_011527024.1:p.Gln282del
XM_011528723.1:c.843_845del	XP_011527025.1:p.Gln282del
XM_011528724.1:c.843_845del	XP_011527026.1:p.Gln282del
XM_011528725.1:c.828_830del	XP_011527027.1:p.Gln277del
XM_011528726.1:c.843_845del	XP_011527028.1:p.Gln282del
XM_011528726.3:c.843_845del	XP_011527028.1:p.Gln282del
XM_011528727.1:c.843_845del	XP_011527029.1:p.Gln282del
XM_011528727.3:c.843_845del	XP_011527029.1:p.Gln282del
XM_011528728.1:c.843_845del	XP_011527030.1:p.Gln282del
XM_011528729.1:c.699_701del	XP_011527031.1:p.Gln234del
XM_011528730.1:c.843_845del	XP_011527032.1:p.Gln282del
XM_011528731.1:c.303_305del	XP_011527033.1:p.Gln102del
XM_011528732.1:c.843_845del	XP_011527034.1:p.Gln282del
XM_011528733.1:c.843_845del	XP_011527035.1:p.Gln282del
XM_011528734.1:c.843_845del	XP_011527036.1:p.Gln282del
XM_011528735.1:c.843_845del	XP_011527037.1:p.Gln282del
XM_017027739.1:c.843_845del	XP_016883228.1:p.Gln282del
XM_017027740.2:c.843_845del	XP_016883229.1:p.Gln282del
XM_017027741.1:c.843_845del	XP_016883230.1:p.Gln282del
XM_017027742.2:c.828_830del	XP_016883231.1:p.Gln277del
XM_017027743.2:c.843_845del	XP_016883232.1:p.Gln282del
XM_017027744.2:c.828_830del	XP_016883233.1:p.Gln277del
XM_017027745.2:c.699_701del	XP_016883234.1:p.Gln234del
XM_017027746.1:c.843_845del	XP_016883235.1:p.Gln282del
XM_017027747.2:c.303_305del	XP_016883236.1:p.Gln102del
XM_017027748.1:c.843_845del	XP_016883237.1:p.Gln282del
XM_017027749.1:c.843_845del	XP_016883238.1:p.Gln282del
XM_017027750.2:c.843_845del	XP_016883239.1:p.Gln282del
XM_017027751.1:c.828_830del	XP_016883240.1:p.Gln277del
XR_001754214.2:n.1114_1116del
XR_001754215.2:n.1114_1116del
XR_936514.1:n.1114_1116del
XR_936515.1:n.1114_1116del