Canonical Allele Identifier: CA2586967385

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589810_154589812del , CM000663.2:g.154589810_154589812del	GRCh38
NC_000001.10:g.154562286_154562288del , CM000663.1:g.154562286_154562288del	GRCh37
NC_000001.9:g.152828910_152828912del	NCBI36
NG_011844.1:g.43153_43155del
NG_011844.2:g.46752_46754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2510_2512del	ENSP00000497790.2:n.2510_2512del
ENST00000649724.2:c.2646_2648del	ENSP00000497932.2:p.Ile883del
ENST00000680270.2:c.2499_2501del	ENSP00000505532.2:p.Ile834del
ENST00000681056.2:c.2268_2270del	ENSP00000506234.2:p.Ile757del
ENST00000368471.8:c.1731_1733del	ENSP00000357456.3:p.Ile578del
ENST00000368474.9:c.2616_2618del MANE Select	ENSP00000357459.4:p.Ile873del
ENST00000529168.2:c.2538_2540del	ENSP00000431794.2:p.Ile847del
ENST00000647682.2:n.2601_2603del
ENST00000648231.2:c.1731_1733del	ENSP00000497555.1:p.Ile578del
ENST00000648311.1:c.1731_1733del	ENSP00000498137.1:p.Ile578del
ENST00000648714.2:c.*91_*93del	ENSP00000497434.2:n.*91_*93del
ENST00000649021.1:n.2652_2654del
ENST00000649022.2:c.1731_1733del	ENSP00000496896.2:p.Ile578del
ENST00000649042.1:c.1731_1733del	ENSP00000497790.1:p.Ile578del
ENST00000649408.2:c.2616_2618del	ENSP00000497386.2:p.Ile873del
ENST00000649724.1:c.1731_1733del	ENSP00000497932.1:p.Ile578del
ENST00000649749.1:c.1731_1733del	ENSP00000497210.1:p.Ile578del
ENST00000679375.1:c.*848_*850del	ENSP00000505887.1:n.*848_*850del
ENST00000679465.1:n.3069_3071del
ENST00000679805.1:n.2652_2654del
ENST00000679899.1:c.1674_1676del	ENSP00000505996.1:p.Ile559del
ENST00000680270.1:c.1731_1733del	ENSP00000505532.1:p.Ile578del
ENST00000680305.1:c.2616_2618del	ENSP00000506312.1:p.Ile873del
ENST00000681056.1:c.1731_1733del	ENSP00000506234.1:p.Ile578del
ENST00000681235.1:c.*2138_*2140del	ENSP00000506606.1:n.*2138_*2140del
ENST00000681429.1:n.1876_1878del
ENST00000681683.1:c.1731_1733del	ENSP00000506666.1:p.Ile578del
ENST00000681786.1:n.3069_3071del
ENST00000681901.1:c.*2216_*2218del	ENSP00000504883.1:n.*2216_*2218del
ENST00000368471.7:c.1731_1733del	ENSP00000357456.3:p.Ile578del
ENST00000368474.8:c.2616_2618del	ENSP00000357459.4:p.Ile873del
ENST00000529168.1:c.2523_2525del	ENSP00000431794.1:p.Ile842del
NM_001025107.2:c.1731_1733del	NP_001020278.1:p.Ile578del
NM_001111.4:c.2616_2618del	NP_001102.2:p.Ile873del
NM_001193495.1:c.1731_1733del	NP_001180424.1:p.Ile578del
NM_015840.3:c.2538_2540del	NP_056655.2:p.Ile847del
NM_015841.3:c.2481_2483del	NP_056656.2:p.Ile828del
XM_006711109.1:c.2646_2648del	XP_006711172.1:p.Ile883del
XM_006711111.2:c.1731_1733del	XP_006711174.1:p.Ile578del
XM_006711112.1:c.1731_1733del	XP_006711175.1:p.Ile578del
XM_006711113.1:c.1731_1733del	XP_006711176.1:p.Ile578del
XM_011509060.1:c.2745_2747del	XP_011507362.1:p.Ile916del
XM_011509061.1:c.2667_2669del	XP_011507363.1:p.Ile890del
XM_011509062.1:c.2634_2636del	XP_011507364.1:p.Ile879del
NM_001025107.3:c.1731_1733del	NP_001020278.1:p.Ile578del
NM_001111.5:c.2616_2618del MANE Select	NP_001102.3:p.Ile873del
NM_001193495.2:c.1731_1733del	NP_001180424.1:p.Ile578del
NM_001365045.1:c.2643_2645del	NP_001351974.1:p.Ile882del
NM_001365046.1:c.1731_1733del	NP_001351975.1:p.Ile578del
NM_001365047.1:c.1731_1733del	NP_001351976.1:p.Ile578del
NM_001365048.1:c.1731_1733del	NP_001351977.1:p.Ile578del
NM_001365049.1:c.1653_1655del	NP_001351978.1:p.Ile552del
NM_015840.4:c.2538_2540del	NP_056655.3:p.Ile847del
NM_015841.4:c.2481_2483del	NP_056656.3:p.Ile828del
XM_006711113.2:c.1731_1733del	XP_006711176.1:p.Ile578del
XM_011509061.2:c.1653_1655del	XP_011507363.2:p.Ile552del
XM_024449674.1:c.2745_2747del	XP_024305442.1:p.Ile916del