Canonical Allele Identifier: CA2586967383

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589788del , CM000663.2:g.154589788del	GRCh38
NC_000001.10:g.154562264del , CM000663.1:g.154562264del	GRCh37
NC_000001.9:g.152828888del	NCBI36
NG_011844.1:g.43175del
NG_011844.2:g.46774del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2532del	ENSP00000497790.2:n.2532del
ENST00000649724.2:c.2668del	ENSP00000497932.2:p.Asp890ThrfsTer15
ENST00000680270.2:c.2521del	ENSP00000505532.2:p.Asp841ThrfsTer15
ENST00000681056.2:c.2290del	ENSP00000506234.2:p.Asp764ThrfsTer15
ENST00000368471.8:c.1753del	ENSP00000357456.3:p.Asp585ThrfsTer15
ENST00000368474.9:c.2638del MANE Select	ENSP00000357459.4:p.Asp880ThrfsTer15
ENST00000529168.2:c.2560del	ENSP00000431794.2:p.Asp854ThrfsTer15
ENST00000647682.2:n.2623del
ENST00000648231.2:c.1753del	ENSP00000497555.1:p.Asp585ThrfsTer15
ENST00000648311.1:c.1753del	ENSP00000498137.1:p.Asp585ThrfsTer15
ENST00000648714.2:c.*113del	ENSP00000497434.2:n.*113del
ENST00000649021.1:n.2674del
ENST00000649022.2:c.1753del	ENSP00000496896.2:p.Asp585ThrfsTer15
ENST00000649042.1:c.1753del	ENSP00000497790.1:p.Asp585ThrfsTer15
ENST00000649408.2:c.2638del	ENSP00000497386.2:p.Asp880ThrfsTer15
ENST00000649724.1:c.1753del	ENSP00000497932.1:p.Asp585ThrfsTer15
ENST00000649749.1:c.1753del	ENSP00000497210.1:p.Asp585ThrfsTer15
ENST00000679375.1:c.*870del	ENSP00000505887.1:n.*870del
ENST00000679465.1:n.3091del
ENST00000679805.1:n.2674del
ENST00000679899.1:c.1696del	ENSP00000505996.1:p.Asp566ThrfsTer15
ENST00000680270.1:c.1753del	ENSP00000505532.1:p.Asp585ThrfsTer15
ENST00000680305.1:c.2638del	ENSP00000506312.1:p.Asp880ThrfsTer15
ENST00000681056.1:c.1753del	ENSP00000506234.1:p.Asp585ThrfsTer15
ENST00000681235.1:c.*2160del	ENSP00000506606.1:n.*2160del
ENST00000681429.1:n.1898del
ENST00000681683.1:c.1753del	ENSP00000506666.1:p.Asp585ThrfsTer15
ENST00000681786.1:n.3091del
ENST00000681901.1:c.*2238del	ENSP00000504883.1:n.*2238del
ENST00000368471.7:c.1753del	ENSP00000357456.3:p.Asp585ThrfsTer15
ENST00000368474.8:c.2638del	ENSP00000357459.4:p.Asp880ThrfsTer15
ENST00000529168.1:c.2545del	ENSP00000431794.1:p.Asp849ThrfsTer15
NM_001025107.2:c.1753del	NP_001020278.1:p.Asp585ThrfsTer15
NM_001111.4:c.2638del	NP_001102.2:p.Asp880ThrfsTer15
NM_001193495.1:c.1753del	NP_001180424.1:p.Asp585ThrfsTer15
NM_015840.3:c.2560del	NP_056655.2:p.Asp854ThrfsTer15
NM_015841.3:c.2503del	NP_056656.2:p.Asp835ThrfsTer15
XM_006711109.1:c.2668del	XP_006711172.1:p.Asp890ThrfsTer15
XM_006711111.2:c.1753del	XP_006711174.1:p.Asp585ThrfsTer15
XM_006711112.1:c.1753del	XP_006711175.1:p.Asp585ThrfsTer15
XM_006711113.1:c.1753del	XP_006711176.1:p.Asp585ThrfsTer15
XM_011509060.1:c.2767del	XP_011507362.1:p.Asp923ThrfsTer15
XM_011509061.1:c.2689del	XP_011507363.1:p.Asp897ThrfsTer15
XM_011509062.1:c.2656del	XP_011507364.1:p.Asp886ThrfsTer15
NM_001025107.3:c.1753del	NP_001020278.1:p.Asp585ThrfsTer15
NM_001111.5:c.2638del MANE Select	NP_001102.3:p.Asp880ThrfsTer15
NM_001193495.2:c.1753del	NP_001180424.1:p.Asp585ThrfsTer15
NM_001365045.1:c.2665del	NP_001351974.1:p.Asp889ThrfsTer15
NM_001365046.1:c.1753del	NP_001351975.1:p.Asp585ThrfsTer15
NM_001365047.1:c.1753del	NP_001351976.1:p.Asp585ThrfsTer15
NM_001365048.1:c.1753del	NP_001351977.1:p.Asp585ThrfsTer15
NM_001365049.1:c.1675del	NP_001351978.1:p.Asp559ThrfsTer15
NM_015840.4:c.2560del	NP_056655.3:p.Asp854ThrfsTer15
NM_015841.4:c.2503del	NP_056656.3:p.Asp835ThrfsTer15
XM_006711113.2:c.1753del	XP_006711176.1:p.Asp585ThrfsTer15
XM_011509061.2:c.1675del	XP_011507363.2:p.Asp559ThrfsTer15
XM_024449674.1:c.2767del	XP_024305442.1:p.Asp923ThrfsTer15