Canonical Allele Identifier: CA2480933207

Gene: ADAR

Linked Data

• dbSNP Id: rs1697006538

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589790_154589791del , CM000663.2:g.154589790_154589791del	GRCh38
NC_000001.10:g.154562266_154562267del , CM000663.1:g.154562266_154562267del	GRCh37
NC_000001.9:g.152828890_152828891del	NCBI36
NG_011844.1:g.43171_43172del
NG_011844.2:g.46770_46771del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2528_2529del	ENSP00000497790.2:n.2528_2529del
ENST00000649724.2:c.2664_2665del	ENSP00000497932.2:p.Glu889GlyfsTer29
ENST00000680270.2:c.2517_2518del	ENSP00000505532.2:p.Glu840GlyfsTer29
ENST00000681056.2:c.2286_2287del	ENSP00000506234.2:p.Glu763GlyfsTer29
ENST00000368471.8:c.1749_1750del	ENSP00000357456.3:p.Glu584GlyfsTer29
ENST00000368474.9:c.2634_2635del MANE Select	ENSP00000357459.4:p.Glu879GlyfsTer29
ENST00000529168.2:c.2556_2557del	ENSP00000431794.2:p.Glu853GlyfsTer29
ENST00000647682.2:n.2619_2620del
ENST00000648231.2:c.1749_1750del	ENSP00000497555.1:p.Glu584GlyfsTer29
ENST00000648311.1:c.1749_1750del	ENSP00000498137.1:p.Glu584GlyfsTer29
ENST00000648714.2:c.*109_*110del	ENSP00000497434.2:n.*109_*110del
ENST00000649021.1:n.2670_2671del
ENST00000649022.2:c.1749_1750del	ENSP00000496896.2:p.Glu584GlyfsTer29
ENST00000649042.1:c.1749_1750del	ENSP00000497790.1:p.Glu584GlyfsTer29
ENST00000649408.2:c.2634_2635del	ENSP00000497386.2:p.Glu879GlyfsTer29
ENST00000649724.1:c.1749_1750del	ENSP00000497932.1:p.Glu584GlyfsTer29
ENST00000649749.1:c.1749_1750del	ENSP00000497210.1:p.Glu584GlyfsTer29
ENST00000679375.1:c.*866_*867del	ENSP00000505887.1:n.*866_*867del
ENST00000679465.1:n.3087_3088del
ENST00000679805.1:n.2670_2671del
ENST00000679899.1:c.1692_1693del	ENSP00000505996.1:p.Glu565GlyfsTer29
ENST00000680270.1:c.1749_1750del	ENSP00000505532.1:p.Glu584GlyfsTer29
ENST00000680305.1:c.2634_2635del	ENSP00000506312.1:p.Glu879GlyfsTer29
ENST00000681056.1:c.1749_1750del	ENSP00000506234.1:p.Glu584GlyfsTer29
ENST00000681235.1:c.*2156_*2157del	ENSP00000506606.1:n.*2156_*2157del
ENST00000681429.1:n.1894_1895del
ENST00000681683.1:c.1749_1750del	ENSP00000506666.1:p.Glu584GlyfsTer29
ENST00000681786.1:n.3087_3088del
ENST00000681901.1:c.*2234_*2235del	ENSP00000504883.1:n.*2234_*2235del
ENST00000368471.7:c.1749_1750del	ENSP00000357456.3:p.Glu584GlyfsTer29
ENST00000368474.8:c.2634_2635del	ENSP00000357459.4:p.Glu879GlyfsTer29
ENST00000529168.1:c.2541_2542del	ENSP00000431794.1:p.Glu848GlyfsTer29
NM_001025107.2:c.1749_1750del	NP_001020278.1:p.Glu584GlyfsTer29
NM_001111.4:c.2634_2635del	NP_001102.2:p.Glu879GlyfsTer29
NM_001193495.1:c.1749_1750del	NP_001180424.1:p.Glu584GlyfsTer29
NM_015840.3:c.2556_2557del	NP_056655.2:p.Glu853GlyfsTer29
NM_015841.3:c.2499_2500del	NP_056656.2:p.Glu834GlyfsTer29
XM_006711109.1:c.2664_2665del	XP_006711172.1:p.Glu889GlyfsTer29
XM_006711111.2:c.1749_1750del	XP_006711174.1:p.Glu584GlyfsTer29
XM_006711112.1:c.1749_1750del	XP_006711175.1:p.Glu584GlyfsTer29
XM_006711113.1:c.1749_1750del	XP_006711176.1:p.Glu584GlyfsTer29
XM_011509060.1:c.2763_2764del	XP_011507362.1:p.Glu922GlyfsTer29
XM_011509061.1:c.2685_2686del	XP_011507363.1:p.Glu896GlyfsTer29
XM_011509062.1:c.2652_2653del	XP_011507364.1:p.Glu885GlyfsTer29
NM_001025107.3:c.1749_1750del	NP_001020278.1:p.Glu584GlyfsTer29
NM_001111.5:c.2634_2635del MANE Select	NP_001102.3:p.Glu879GlyfsTer29
NM_001193495.2:c.1749_1750del	NP_001180424.1:p.Glu584GlyfsTer29
NM_001365045.1:c.2661_2662del	NP_001351974.1:p.Glu888GlyfsTer29
NM_001365046.1:c.1749_1750del	NP_001351975.1:p.Glu584GlyfsTer29
NM_001365047.1:c.1749_1750del	NP_001351976.1:p.Glu584GlyfsTer29
NM_001365048.1:c.1749_1750del	NP_001351977.1:p.Glu584GlyfsTer29
NM_001365049.1:c.1671_1672del	NP_001351978.1:p.Glu558GlyfsTer29
NM_015840.4:c.2556_2557del	NP_056655.3:p.Glu853GlyfsTer29
NM_015841.4:c.2499_2500del	NP_056656.3:p.Glu834GlyfsTer29
XM_006711113.2:c.1749_1750del	XP_006711176.1:p.Glu584GlyfsTer29
XM_011509061.2:c.1671_1672del	XP_011507363.2:p.Glu558GlyfsTer29
XM_024449674.1:c.2763_2764del	XP_024305442.1:p.Glu922GlyfsTer29