Canonical Allele Identifier: CA2570271887

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589669_154589670insAAGCTTTCA , CM000663.2:g.154589669_154589670insAAGCTTTCA	GRCh38
NC_000001.10:g.154562145_154562146insAAGCTTTCA , CM000663.1:g.154562145_154562146insAAGCTTTCA	GRCh37
NC_000001.9:g.152828769_152828770insAAGCTTTCA	NCBI36
NG_011844.1:g.43292_43293insTGAAAGCTT
NG_011844.2:g.46891_46892insTGAAAGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2562+87_2562+88insTGAAAGCTT	ENSP00000497790.2:n.2562+87_2562+88insTGAAAGCTT
ENST00000649724.2:c.2698+87_2698+88insTGAAAGCTT	ENSP00000497932.2:n.2698+87_2698+88insTGAAAGCTT
ENST00000680270.2:c.2551+87_2551+88insTGAAAGCTT	ENSP00000505532.2:n.2551+87_2551+88insTGAAAGCTT
ENST00000681056.2:c.2320+87_2320+88insTGAAAGCTT	ENSP00000506234.2:n.2320+87_2320+88insTGAAAGCTT
ENST00000368471.8:c.1783+87_1783+88insTGAAAGCTT	ENSP00000357456.3:n.1783+87_1783+88insTGAAAGCTT
ENST00000368474.9:c.2668+87_2668+88insTGAAAGCTT MANE Select	ENSP00000357459.4:n.2668+87_2668+88insTGAAAGCTT
ENST00000529168.2:c.2590+87_2590+88insTGAAAGCTT	ENSP00000431794.2:n.2590+87_2590+88insTGAAAGCTT
ENST00000647682.2:n.2653+87_2653+88insTGAAAGCTT
ENST00000648231.2:c.1783+87_1783+88insTGAAAGCTT	ENSP00000497555.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000648311.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000498137.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000648714.2:c.*143+87_*143+88insTGAAAGCTT	ENSP00000497434.2:n.*143+87_*143+88insTGAAAGCTT
ENST00000649021.1:n.2704+87_2704+88insTGAAAGCTT
ENST00000649022.2:c.1783+87_1783+88insTGAAAGCTT	ENSP00000496896.2:n.1783+87_1783+88insTGAAAGCTT
ENST00000649042.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000497790.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000649408.2:c.2668+87_2668+88insTGAAAGCTT	ENSP00000497386.2:n.2668+87_2668+88insTGAAAGCTT
ENST00000649724.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000497932.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000649749.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000497210.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000679375.1:c.*900+87_*900+88insTGAAAGCTT	ENSP00000505887.1:n.*900+87_*900+88insTGAAAGCTT
ENST00000679465.1:n.3121+87_3121+88insTGAAAGCTT
ENST00000679805.1:n.2704+87_2704+88insTGAAAGCTT
ENST00000679899.1:c.1726+87_1726+88insTGAAAGCTT	ENSP00000505996.1:n.1726+87_1726+88insTGAAAGCTT
ENST00000680270.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000505532.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000680305.1:c.2668+87_2668+88insTGAAAGCTT	ENSP00000506312.1:n.2668+87_2668+88insTGAAAGCTT
ENST00000681056.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000506234.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000681235.1:c.*2190+87_*2190+88insTGAAAGCTT	ENSP00000506606.1:n.*2190+87_*2190+88insTGAAAGCTT
ENST00000681429.1:n.1928+87_1928+88insTGAAAGCTT
ENST00000681683.1:c.1783+87_1783+88insTGAAAGCTT	ENSP00000506666.1:n.1783+87_1783+88insTGAAAGCTT
ENST00000681786.1:n.3121+87_3121+88insTGAAAGCTT
ENST00000681901.1:c.*2268+87_*2268+88insTGAAAGCTT	ENSP00000504883.1:n.*2268+87_*2268+88insTGAAAGCTT
ENST00000368471.7:c.1783+87_1783+88insTGAAAGCTT	ENSP00000357456.3:n.1783+87_1783+88insTGAAAGCTT
ENST00000368474.8:c.2668+87_2668+88insTGAAAGCTT	ENSP00000357459.4:n.2668+87_2668+88insTGAAAGCTT
ENST00000529168.1:c.2575+87_2575+88insTGAAAGCTT	ENSP00000431794.1:n.2575+87_2575+88insTGAAAGCTT
NM_001025107.2:c.1783+87_1783+88insTGAAAGCTT	NP_001020278.1:n.1783+87_1783+88insTGAAAGCTT
NM_001111.4:c.2668+87_2668+88insTGAAAGCTT	NP_001102.2:n.2668+87_2668+88insTGAAAGCTT
NM_001193495.1:c.1783+87_1783+88insTGAAAGCTT	NP_001180424.1:n.1783+87_1783+88insTGAAAGCTT
NM_015840.3:c.2590+87_2590+88insTGAAAGCTT	NP_056655.2:n.2590+87_2590+88insTGAAAGCTT
NM_015841.3:c.2533+87_2533+88insTGAAAGCTT	NP_056656.2:n.2533+87_2533+88insTGAAAGCTT
XM_006711109.1:c.2698+87_2698+88insTGAAAGCTT	XP_006711172.1:n.2698+87_2698+88insTGAAAGCTT
XM_006711111.2:c.1783+87_1783+88insTGAAAGCTT	XP_006711174.1:n.1783+87_1783+88insTGAAAGCTT
XM_006711112.1:c.1783+87_1783+88insTGAAAGCTT	XP_006711175.1:n.1783+87_1783+88insTGAAAGCTT
XM_006711113.1:c.1783+87_1783+88insTGAAAGCTT	XP_006711176.1:n.1783+87_1783+88insTGAAAGCTT
XM_011509060.1:c.2797+87_2797+88insTGAAAGCTT	XP_011507362.1:n.2797+87_2797+88insTGAAAGCTT
XM_011509061.1:c.2719+87_2719+88insTGAAAGCTT	XP_011507363.1:n.2719+87_2719+88insTGAAAGCTT
XM_011509062.1:c.2686+87_2686+88insTGAAAGCTT	XP_011507364.1:n.2686+87_2686+88insTGAAAGCTT
NM_001025107.3:c.1783+87_1783+88insTGAAAGCTT	NP_001020278.1:n.1783+87_1783+88insTGAAAGCTT
NM_001111.5:c.2668+87_2668+88insTGAAAGCTT MANE Select	NP_001102.3:n.2668+87_2668+88insTGAAAGCTT
NM_001193495.2:c.1783+87_1783+88insTGAAAGCTT	NP_001180424.1:n.1783+87_1783+88insTGAAAGCTT
NM_001365045.1:c.2695+87_2695+88insTGAAAGCTT	NP_001351974.1:n.2695+87_2695+88insTGAAAGCTT
NM_001365046.1:c.1783+87_1783+88insTGAAAGCTT	NP_001351975.1:n.1783+87_1783+88insTGAAAGCTT
NM_001365047.1:c.1783+87_1783+88insTGAAAGCTT	NP_001351976.1:n.1783+87_1783+88insTGAAAGCTT
NM_001365048.1:c.1783+87_1783+88insTGAAAGCTT	NP_001351977.1:n.1783+87_1783+88insTGAAAGCTT
NM_001365049.1:c.1705+87_1705+88insTGAAAGCTT	NP_001351978.1:n.1705+87_1705+88insTGAAAGCTT
NM_015840.4:c.2590+87_2590+88insTGAAAGCTT	NP_056655.3:n.2590+87_2590+88insTGAAAGCTT
NM_015841.4:c.2533+87_2533+88insTGAAAGCTT	NP_056656.3:n.2533+87_2533+88insTGAAAGCTT
XM_006711113.2:c.1783+87_1783+88insTGAAAGCTT	XP_006711176.1:n.1783+87_1783+88insTGAAAGCTT
XM_011509061.2:c.1705+87_1705+88insTGAAAGCTT	XP_011507363.2:n.1705+87_1705+88insTGAAAGCTT
XM_024449674.1:c.2797+87_2797+88insTGAAAGCTT	XP_024305442.1:n.2797+87_2797+88insTGAAAGCTT