Canonical Allele Identifier: CA1864173482

Gene: NOL8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92301665C= , CM000671.2:g.92301665C=	GRCh38
NC_000009.11:g.95063947C= , CM000671.1:g.95063947C=	GRCh37
NC_000009.10:g.94103768C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442668.7:c.3061G= MANE Select	ENSP00000401177.2:p.Gly1021=
ENST00000358855.8:c.2857G=	ENSP00000351723.4:p.Gly953=
ENST00000360868.7:c.*2916G=	ENSP00000354115.3:n.*2916G=
ENST00000442668.6:c.3061G=	ENSP00000401177.2:p.Gly1021=
ENST00000477862.1:n.421G=
ENST00000535387.5:c.2947G=	ENSP00000441300.1:p.Gly983=
ENST00000536593.5:c.*2916G=	ENSP00000446265.1:n.*2916G=
ENST00000542053.5:c.2857G=	ENSP00000440709.1:p.Gly953=
ENST00000544867.5:c.3061G=	ENSP00000439751.1:p.Gly1021=
ENST00000545444.5:c.*591G=	ENSP00000439829.1:n.*591G=
ENST00000545558.5:c.3061G=	ENSP00000441140.1:p.Gly1021=
NM_001256394.1:c.2857G=	NP_001243323.1:p.Gly953=
NM_017948.5:c.3061G=	NP_060418.4:p.Gly1021=
NR_046106.1:n.3398G=
XM_006717166.2:c.3061G=	XP_006717229.1:p.Gly1021=
XM_006717167.2:c.3061G=	XP_006717230.1:p.Gly1021=
XM_006717168.2:c.2947G=	XP_006717231.1:p.Gly983=
XM_006717169.2:c.2857G=	XP_006717232.1:p.Gly953=
XM_006717170.2:c.2857G=	XP_006717233.1:p.Gly953=
XM_006717172.2:c.2683G=	XP_006717235.1:p.Gly895=
XM_006717173.2:c.2683G=	XP_006717236.1:p.Gly895=
XM_011518824.1:c.2857G=	XP_011517126.1:p.Gly953=
XM_011518825.1:c.2857G=	XP_011517127.1:p.Gly953=
XM_011518826.1:c.3061G=	XP_011517128.1:p.Gly1021=
XM_011518827.1:c.2683G=	XP_011517129.1:p.Gly895=
XM_011518828.1:c.2458G=	XP_011517130.1:p.Gly820=
NM_001330722.1:c.2947G=	NP_001317651.1:p.Gly983=
XM_006717166.4:c.3061G=	XP_006717229.1:p.Gly1021=
XM_006717167.3:c.3061G=	XP_006717230.1:p.Gly1021=
XM_006717169.4:c.2857G=	XP_006717232.1:p.Gly953=
XM_006717170.4:c.2857G=	XP_006717233.1:p.Gly953=
XM_006717172.4:c.2683G=	XP_006717235.1:p.Gly895=
XM_006717173.4:c.2683G=	XP_006717236.1:p.Gly895=
XM_011518824.3:c.2857G=	XP_011517126.1:p.Gly953=
XM_011518827.2:c.2683G=	XP_011517129.1:p.Gly895=
XM_017014876.2:c.2947G=	XP_016870365.1:p.Gly983=
XM_017014877.2:c.2743G=	XP_016870366.1:p.Gly915=
XM_017014878.2:c.2683G=	XP_016870367.1:p.Gly895=
XM_017014879.1:c.2683G=	XP_016870368.1:p.Gly895=
XM_017014880.2:c.2569G=	XP_016870369.1:p.Gly857=
XM_024447594.1:c.2857G=	XP_024303362.1:p.Gly953=
XM_024447595.1:c.2683G=	XP_024303363.1:p.Gly895=
XR_001746333.2:n.3162G=
XR_001746334.2:n.3289G=
NM_017948.6:c.3061G= MANE Select	NP_060418.4:p.Gly1021=
NM_001256394.2:c.2857G=	NP_001243323.1:p.Gly953=
NM_001330722.2:c.2947G=	NP_001317651.1:p.Gly983=
NR_046106.2:n.3154G=