Canonical Allele Identifier: CA9823682

Gene: NCOA6

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34743271T>G , CM000682.2:g.34743271T>G	GRCh38
NC_000020.10:g.33331075T>G , CM000682.1:g.33331075T>G	GRCh37
NC_000020.9:g.32794736T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359003.7:c.2985A>C MANE Select	ENSP00000351894.2:p.Ala995=
ENST00000359003.6:c.2985A>C	ENSP00000351894.2:p.Ala995=
ENST00000374796.6:c.2985A>C	ENSP00000363929.2:p.Ala995=
ENST00000612493.4:c.2914+3536A>C	ENSP00000481177.1:n.2914+3536A>C
ENST00000616167.1:c.2914+3536A>C	ENSP00000481935.1:n.2914+3536A>C
ENST00000628752.2:c.302+3536A>C
NM_001242539.1:c.2914+3536A>C	NP_001229468.1:n.2914+3536A>C
NM_014071.3:c.2985A>C	NP_054790.2:p.Ala995=
XM_006723755.2:c.2985A>C	XP_006723818.1:p.Ala995=
XM_011528721.1:c.3000A>C	XP_011527023.1:p.Ala1000=
XM_011528722.1:c.3000A>C	XP_011527024.1:p.Ala1000=
XM_011528723.1:c.3000A>C	XP_011527025.1:p.Ala1000=
XM_011528724.1:c.3000A>C	XP_011527026.1:p.Ala1000=
XM_011528725.1:c.2985A>C	XP_011527027.1:p.Ala995=
XM_011528726.1:c.2967A>C	XP_011527028.1:p.Ala989=
XM_011528727.1:c.2964A>C	XP_011527029.1:p.Ala988=
XM_011528728.1:c.3000A>C	XP_011527030.1:p.Ala1000=
XM_011528729.1:c.2856A>C	XP_011527031.1:p.Ala952=
XM_011528730.1:c.3000A>C	XP_011527032.1:p.Ala1000=
XM_011528731.1:c.2460A>C	XP_011527033.1:p.Ala820=
XM_011528732.1:c.3000A>C	XP_011527034.1:p.Ala1000=
XM_011528733.1:c.3000A>C	XP_011527035.1:p.Ala1000=
XM_011528734.1:c.3000A>C	XP_011527036.1:p.Ala1000=
XM_011528735.1:c.2929+3536A>C	XP_011527037.1:n.2929+3536A>C
XR_936514.1:n.3271A>C
XR_936515.1:n.3271A>C
NM_001242539.2:c.2914+3536A>C	NP_001229468.1:n.2914+3536A>C
NM_001318240.1:c.2985A>C	NP_001305169.1:p.Ala995=
NM_014071.4:c.2985A>C	NP_054790.2:p.Ala995=
XM_006723755.3:c.2985A>C	XP_006723818.1:p.Ala995=
XM_011528721.3:c.3000A>C	XP_011527023.1:p.Ala1000=
XM_011528726.3:c.2967A>C	XP_011527028.1:p.Ala989=
XM_011528727.3:c.2964A>C	XP_011527029.1:p.Ala988=
XM_017027739.1:c.3057A>C	XP_016883228.1:p.Ala1019=
XM_017027740.2:c.3057A>C	XP_016883229.1:p.Ala1019=
XM_017027741.1:c.3057A>C	XP_016883230.1:p.Ala1019=
XM_017027742.2:c.3042A>C	XP_016883231.1:p.Ala1014=
XM_017027743.2:c.3057A>C	XP_016883232.1:p.Ala1019=
XM_017027744.2:c.2949A>C	XP_016883233.1:p.Ala983=
XM_017027745.2:c.2913A>C	XP_016883234.1:p.Ala971=
XM_017027746.1:c.3057A>C	XP_016883235.1:p.Ala1019=
XM_017027747.2:c.2517A>C	XP_016883236.1:p.Ala839=
XM_017027748.1:c.3057A>C	XP_016883237.1:p.Ala1019=
XM_017027749.1:c.3057A>C	XP_016883238.1:p.Ala1019=
XM_017027750.2:c.2986+3536A>C	XP_016883239.1:n.2986+3536A>C
XM_017027751.1:c.2914+3536A>C	XP_016883240.1:n.2914+3536A>C
XR_001754214.2:n.3328A>C
XR_001754215.2:n.3328A>C
NM_014071.5:c.2985A>C MANE Select	NP_054790.2:p.Ala995=