Canonical Allele Identifier: CA2573914367

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589806_154589808del , CM000663.2:g.154589806_154589808del	GRCh38
NC_000001.10:g.154562282_154562284del , CM000663.1:g.154562282_154562284del	GRCh37
NC_000001.9:g.152828906_152828908del	NCBI36
NG_011844.1:g.43156_43158del
NG_011844.2:g.46755_46757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2513_2515del	ENSP00000497790.2:n.2513_2515del
ENST00000649724.2:c.2649_2651del	ENSP00000497932.2:p.Ile883del
ENST00000680270.2:c.2502_2504del	ENSP00000505532.2:p.Ile834del
ENST00000681056.2:c.2271_2273del	ENSP00000506234.2:p.Ile757del
ENST00000368471.8:c.1734_1736del	ENSP00000357456.3:p.Ile578del
ENST00000368474.9:c.2619_2621del MANE Select	ENSP00000357459.4:p.Ile873del
ENST00000529168.2:c.2541_2543del	ENSP00000431794.2:p.Ile847del
ENST00000647682.2:n.2604_2606del
ENST00000648231.2:c.1734_1736del	ENSP00000497555.1:p.Ile578del
ENST00000648311.1:c.1734_1736del	ENSP00000498137.1:p.Ile578del
ENST00000648714.2:c.*94_*96del	ENSP00000497434.2:n.*94_*96del
ENST00000649021.1:n.2655_2657del
ENST00000649022.2:c.1734_1736del	ENSP00000496896.2:p.Ile578del
ENST00000649042.1:c.1734_1736del	ENSP00000497790.1:p.Ile578del
ENST00000649408.2:c.2619_2621del	ENSP00000497386.2:p.Ile873del
ENST00000649724.1:c.1734_1736del	ENSP00000497932.1:p.Ile578del
ENST00000649749.1:c.1734_1736del	ENSP00000497210.1:p.Ile578del
ENST00000679375.1:c.*851_*853del	ENSP00000505887.1:n.*851_*853del
ENST00000679465.1:n.3072_3074del
ENST00000679805.1:n.2655_2657del
ENST00000679899.1:c.1677_1679del	ENSP00000505996.1:p.Ile559del
ENST00000680270.1:c.1734_1736del	ENSP00000505532.1:p.Ile578del
ENST00000680305.1:c.2619_2621del	ENSP00000506312.1:p.Ile873del
ENST00000681056.1:c.1734_1736del	ENSP00000506234.1:p.Ile578del
ENST00000681235.1:c.*2141_*2143del	ENSP00000506606.1:n.*2141_*2143del
ENST00000681429.1:n.1879_1881del
ENST00000681683.1:c.1734_1736del	ENSP00000506666.1:p.Ile578del
ENST00000681786.1:n.3072_3074del
ENST00000681901.1:c.*2219_*2221del	ENSP00000504883.1:n.*2219_*2221del
ENST00000368471.7:c.1734_1736del	ENSP00000357456.3:p.Ile578del
ENST00000368474.8:c.2619_2621del	ENSP00000357459.4:p.Ile873del
ENST00000529168.1:c.2526_2528del	ENSP00000431794.1:p.Ile842del
NM_001025107.2:c.1734_1736del	NP_001020278.1:p.Ile578del
NM_001111.4:c.2619_2621del	NP_001102.2:p.Ile873del
NM_001193495.1:c.1734_1736del	NP_001180424.1:p.Ile578del
NM_015840.3:c.2541_2543del	NP_056655.2:p.Ile847del
NM_015841.3:c.2484_2486del	NP_056656.2:p.Ile828del
XM_006711109.1:c.2649_2651del	XP_006711172.1:p.Ile883del
XM_006711111.2:c.1734_1736del	XP_006711174.1:p.Ile578del
XM_006711112.1:c.1734_1736del	XP_006711175.1:p.Ile578del
XM_006711113.1:c.1734_1736del	XP_006711176.1:p.Ile578del
XM_011509060.1:c.2748_2750del	XP_011507362.1:p.Ile916del
XM_011509061.1:c.2670_2672del	XP_011507363.1:p.Ile890del
XM_011509062.1:c.2637_2639del	XP_011507364.1:p.Ile879del
NM_001025107.3:c.1734_1736del	NP_001020278.1:p.Ile578del
NM_001111.5:c.2619_2621del MANE Select	NP_001102.3:p.Ile873del
NM_001193495.2:c.1734_1736del	NP_001180424.1:p.Ile578del
NM_001365045.1:c.2646_2648del	NP_001351974.1:p.Ile882del
NM_001365046.1:c.1734_1736del	NP_001351975.1:p.Ile578del
NM_001365047.1:c.1734_1736del	NP_001351976.1:p.Ile578del
NM_001365048.1:c.1734_1736del	NP_001351977.1:p.Ile578del
NM_001365049.1:c.1656_1658del	NP_001351978.1:p.Ile552del
NM_015840.4:c.2541_2543del	NP_056655.3:p.Ile847del
NM_015841.4:c.2484_2486del	NP_056656.3:p.Ile828del
XM_006711113.2:c.1734_1736del	XP_006711176.1:p.Ile578del
XM_011509061.2:c.1656_1658del	XP_011507363.2:p.Ile552del
XM_024449674.1:c.2748_2750del	XP_024305442.1:p.Ile916del