Canonical Allele Identifier: CA342636590

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589402T>C , CM000663.2:g.154589402T>C	GRCh38
NC_000001.10:g.154561878T>C , CM000663.1:g.154561878T>C	GRCh37
NC_000001.9:g.152828502T>C	NCBI36
NG_011844.1:g.43560A>G
NG_011844.2:g.47159A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.2729A>G MANE Select	NP_001102.3:p.His910Arg
ENST00000368474.9:c.2729A>G MANE Select	ENSP00000357459.4:p.His910Arg
NM_001025107.2:c.1844A>G	NP_001020278.1:p.His615Arg
NM_001025107.3:c.1844A>G	NP_001020278.1:p.His615Arg
NM_001111.4:c.2729A>G	NP_001102.2:p.His910Arg
NM_001193495.1:c.1844A>G	NP_001180424.1:p.His615Arg
NM_001193495.2:c.1844A>G	NP_001180424.1:p.His615Arg
NM_001365045.1:c.2756A>G	NP_001351974.1:p.His919Arg
NM_001365046.1:c.1844A>G	NP_001351975.1:p.His615Arg
NM_001365047.1:c.1844A>G	NP_001351976.1:p.His615Arg
NM_001365048.1:c.1844A>G	NP_001351977.1:p.His615Arg
NM_001365049.1:c.1766A>G	NP_001351978.1:p.His589Arg
NM_015840.3:c.2651A>G	NP_056655.2:p.His884Arg
NM_015840.4:c.2651A>G	NP_056655.3:p.His884Arg
NM_015841.3:c.2594A>G	NP_056656.2:p.His865Arg
NM_015841.4:c.2594A>G	NP_056656.3:p.His865Arg
ENST00000368471.7:c.1844A>G	ENSP00000357456.3:p.His615Arg
ENST00000368471.8:c.1844A>G	ENSP00000357456.3:p.His615Arg
ENST00000368474.8:c.2729A>G	ENSP00000357459.4:p.His910Arg
ENST00000529168.1:c.2636A>G	ENSP00000431794.1:p.His879Arg
ENST00000529168.2:c.2651A>G	ENSP00000431794.2:p.His884Arg
ENST00000647682.2:n.2714A>G
ENST00000648231.2:c.1844A>G	ENSP00000497555.1:p.His615Arg
ENST00000648311.1:c.1844A>G	ENSP00000498137.1:p.His615Arg
ENST00000648714.2:c.*204A>G	ENSP00000497434.2:n.*204A>G
ENST00000649021.1:n.2765A>G
ENST00000649022.2:c.1844A>G	ENSP00000496896.2:p.His615Arg
ENST00000649042.1:c.1844A>G	ENSP00000497790.1:p.His615Arg
ENST00000649042.2:c.2623A>G	ENSP00000497790.2:n.2623A>G
ENST00000649408.2:c.2729A>G	ENSP00000497386.2:p.His910Arg
ENST00000649724.1:c.1844A>G	ENSP00000497932.1:p.His615Arg
ENST00000649724.2:c.2759A>G	ENSP00000497932.2:p.His920Arg
ENST00000649749.1:c.1844A>G	ENSP00000497210.1:p.His615Arg
ENST00000679375.1:c.*961A>G	ENSP00000505887.1:n.*961A>G
ENST00000679465.1:n.3182A>G
ENST00000679805.1:n.2765A>G
ENST00000679899.1:c.1787A>G	ENSP00000505996.1:p.His596Arg
ENST00000680270.1:c.1844A>G	ENSP00000505532.1:p.His615Arg
ENST00000680270.2:c.2612A>G	ENSP00000505532.2:p.His871Arg
ENST00000680305.1:c.2729A>G	ENSP00000506312.1:p.His910Arg
ENST00000681056.1:c.1844A>G	ENSP00000506234.1:p.His615Arg
ENST00000681056.2:c.2381A>G	ENSP00000506234.2:p.His794Arg
ENST00000681235.1:c.*2251A>G	ENSP00000506606.1:n.*2251A>G
ENST00000681429.1:n.1989A>G
ENST00000681683.1:c.1844A>G	ENSP00000506666.1:p.His615Arg
ENST00000681786.1:n.3182A>G
ENST00000681901.1:c.*2329A>G	ENSP00000504883.1:n.*2329A>G
XM_006711109.1:c.2759A>G	XP_006711172.1:p.His920Arg
XM_006711111.2:c.1844A>G	XP_006711174.1:p.His615Arg
XM_006711112.1:c.1844A>G	XP_006711175.1:p.His615Arg
XM_006711113.1:c.1844A>G	XP_006711176.1:p.His615Arg
XM_006711113.2:c.1844A>G	XP_006711176.1:p.His615Arg
XM_011509060.1:c.2858A>G	XP_011507362.1:p.His953Arg
XM_011509061.1:c.2780A>G	XP_011507363.1:p.His927Arg
XM_011509061.2:c.1766A>G	XP_011507363.2:p.His589Arg
XM_011509062.1:c.2747A>G	XP_011507364.1:p.His916Arg
XM_024449674.1:c.2858A>G	XP_024305442.1:p.His953Arg