Canonical Allele Identifier: CA1149071067

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588140T= , CM000663.2:g.154588140T=	GRCh38
NC_000001.10:g.154560616T= , CM000663.1:g.154560616T=	GRCh37
NC_000001.9:g.152827240T=	NCBI36
NG_011844.1:g.44822A=
NG_011844.2:g.48421A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2898A=	ENSP00000497790.2:n.2898A=
ENST00000649724.2:c.3034A=	ENSP00000497932.2:p.Thr1012=
ENST00000680270.2:c.2887A=	ENSP00000505532.2:p.Thr963=
ENST00000681056.2:c.2656A=	ENSP00000506234.2:p.Thr886=
ENST00000368471.8:c.2119A=	ENSP00000357456.3:p.Thr707=
ENST00000368474.9:c.3004A= MANE Select	ENSP00000357459.4:p.Thr1002=
ENST00000529168.2:c.2926A=	ENSP00000431794.2:p.Thr976=
ENST00000647682.2:n.2989A=
ENST00000648231.2:c.2119A=	ENSP00000497555.1:p.Thr707=
ENST00000648311.1:c.2119A=	ENSP00000498137.1:p.Thr707=
ENST00000648714.2:c.*479A=	ENSP00000497434.2:n.*479A=
ENST00000649021.1:n.3332A=
ENST00000649022.2:c.2119A=	ENSP00000496896.2:p.Thr707=
ENST00000649042.1:c.2119A=	ENSP00000497790.1:p.Thr707=
ENST00000649408.2:c.3004A=	ENSP00000497386.2:p.Thr1002=
ENST00000649724.1:c.2119A=	ENSP00000497932.1:p.Thr707=
ENST00000649749.1:c.2119A=	ENSP00000497210.1:p.Thr707=
ENST00000679375.1:c.*1236A=	ENSP00000505887.1:n.*1236A=
ENST00000679465.1:n.3457A=
ENST00000679805.1:n.3332A=
ENST00000679899.1:c.2062A=	ENSP00000505996.1:p.Thr688=
ENST00000680270.1:c.2119A=	ENSP00000505532.1:p.Thr707=
ENST00000680305.1:c.3004A=	ENSP00000506312.1:p.Thr1002=
ENST00000681056.1:c.2119A=	ENSP00000506234.1:p.Thr707=
ENST00000681235.1:c.*2526A=	ENSP00000506606.1:n.*2526A=
ENST00000681429.1:n.2264A=
ENST00000681683.1:c.2119A=	ENSP00000506666.1:p.Thr707=
ENST00000681786.1:n.3457A=
ENST00000681901.1:c.*2604A=	ENSP00000504883.1:n.*2604A=
ENST00000368471.7:c.2119A=	ENSP00000357456.3:p.Thr707=
ENST00000368474.8:c.3004A=	ENSP00000357459.4:p.Thr1002=
ENST00000529168.1:c.2911A=	ENSP00000431794.1:p.Thr971=
ENST00000530954.1:n.141A=
ENST00000534279.1:n.463A=
NM_001025107.2:c.2119A=	NP_001020278.1:p.Thr707=
NM_001111.4:c.3004A=	NP_001102.2:p.Thr1002=
NM_001193495.1:c.2119A=	NP_001180424.1:p.Thr707=
NM_015840.3:c.2926A=	NP_056655.2:p.Thr976=
NM_015841.3:c.2869A=	NP_056656.2:p.Thr957=
XM_006711109.1:c.3034A=	XP_006711172.1:p.Thr1012=
XM_006711111.2:c.2119A=	XP_006711174.1:p.Thr707=
XM_006711112.1:c.2119A=	XP_006711175.1:p.Thr707=
XM_006711113.1:c.2119A=	XP_006711176.1:p.Thr707=
XM_011509060.1:c.3133A=	XP_011507362.1:p.Thr1045=
XM_011509061.1:c.3055A=	XP_011507363.1:p.Thr1019=
XM_011509062.1:c.3022A=	XP_011507364.1:p.Thr1008=
NM_001025107.3:c.2119A=	NP_001020278.1:p.Thr707=
NM_001111.5:c.3004A= MANE Select	NP_001102.3:p.Thr1002=
NM_001193495.2:c.2119A=	NP_001180424.1:p.Thr707=
NM_001365045.1:c.3031A=	NP_001351974.1:p.Thr1011=
NM_001365046.1:c.2119A=	NP_001351975.1:p.Thr707=
NM_001365047.1:c.2119A=	NP_001351976.1:p.Thr707=
NM_001365048.1:c.2119A=	NP_001351977.1:p.Thr707=
NM_001365049.1:c.2041A=	NP_001351978.1:p.Thr681=
NM_015840.4:c.2926A=	NP_056655.3:p.Thr976=
NM_015841.4:c.2869A=	NP_056656.3:p.Thr957=
XM_006711113.2:c.2119A=	XP_006711176.1:p.Thr707=
XM_011509061.2:c.2041A=	XP_011507363.2:p.Thr681=
XM_024449674.1:c.3133A=	XP_024305442.1:p.Thr1045=