Canonical Allele Identifier: CA2648179105

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589384-CGGGAGATTATTTCTGCATGGCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589385_154589407del , CM000663.2:g.154589385_154589407del	GRCh38
NC_000001.10:g.154561861_154561883del , CM000663.1:g.154561861_154561883del	GRCh37
NC_000001.9:g.152828485_152828507del	NCBI36
NG_011844.1:g.43555_43577del
NG_011844.2:g.47154_47176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2618_2640del	ENSP00000497790.2:n.2618_2640del
ENST00000649724.2:c.2754_2776del	ENSP00000497932.2:p.Asp918GlufsTer11
ENST00000680270.2:c.2607_2629del	ENSP00000505532.2:p.Asp869GlufsTer11
ENST00000681056.2:c.2376_2398del	ENSP00000506234.2:p.Asp792GlufsTer11
ENST00000368471.8:c.1839_1861del	ENSP00000357456.3:p.Asp613GlufsTer11
ENST00000368474.9:c.2724_2746del MANE Select	ENSP00000357459.4:p.Asp908GlufsTer11
ENST00000529168.2:c.2646_2668del	ENSP00000431794.2:p.Asp882GlufsTer11
ENST00000647682.2:n.2709_2731del
ENST00000648231.2:c.1839_1861del	ENSP00000497555.1:p.Asp613GlufsTer11
ENST00000648311.1:c.1839_1861del	ENSP00000498137.1:p.Asp613GlufsTer11
ENST00000648714.2:c.*199_*221del	ENSP00000497434.2:n.*199_*221del
ENST00000649021.1:n.2760_2782del
ENST00000649022.2:c.1839_1861del	ENSP00000496896.2:p.Asp613GlufsTer11
ENST00000649042.1:c.1839_1861del	ENSP00000497790.1:p.Asp613GlufsTer11
ENST00000649408.2:c.2724_2746del	ENSP00000497386.2:p.Asp908GlufsTer11
ENST00000649724.1:c.1839_1861del	ENSP00000497932.1:p.Asp613GlufsTer11
ENST00000649749.1:c.1839_1861del	ENSP00000497210.1:p.Asp613GlufsTer11
ENST00000679375.1:c.*956_*978del	ENSP00000505887.1:n.*956_*978del
ENST00000679465.1:n.3177_3199del
ENST00000679805.1:n.2760_2782del
ENST00000679899.1:c.1782_1804del	ENSP00000505996.1:p.Asp594GlufsTer11
ENST00000680270.1:c.1839_1861del	ENSP00000505532.1:p.Asp613GlufsTer11
ENST00000680305.1:c.2724_2746del	ENSP00000506312.1:p.Asp908GlufsTer11
ENST00000681056.1:c.1839_1861del	ENSP00000506234.1:p.Asp613GlufsTer11
ENST00000681235.1:c.*2246_*2268del	ENSP00000506606.1:n.*2246_*2268del
ENST00000681429.1:n.1984_2006del
ENST00000681683.1:c.1839_1861del	ENSP00000506666.1:p.Asp613GlufsTer11
ENST00000681786.1:n.3177_3199del
ENST00000681901.1:c.*2324_*2346del	ENSP00000504883.1:n.*2324_*2346del
ENST00000368471.7:c.1839_1861del	ENSP00000357456.3:p.Asp613GlufsTer11
ENST00000368474.8:c.2724_2746del	ENSP00000357459.4:p.Asp908GlufsTer11
ENST00000529168.1:c.2631_2653del	ENSP00000431794.1:p.Asp877GlufsTer11
NM_001025107.2:c.1839_1861del	NP_001020278.1:p.Asp613GlufsTer11
NM_001111.4:c.2724_2746del	NP_001102.2:p.Asp908GlufsTer11
NM_001193495.1:c.1839_1861del	NP_001180424.1:p.Asp613GlufsTer11
NM_015840.3:c.2646_2668del	NP_056655.2:p.Asp882GlufsTer11
NM_015841.3:c.2589_2611del	NP_056656.2:p.Asp863GlufsTer11
XM_006711109.1:c.2754_2776del	XP_006711172.1:p.Asp918GlufsTer11
XM_006711111.2:c.1839_1861del	XP_006711174.1:p.Asp613GlufsTer11
XM_006711112.1:c.1839_1861del	XP_006711175.1:p.Asp613GlufsTer11
XM_006711113.1:c.1839_1861del	XP_006711176.1:p.Asp613GlufsTer11
XM_011509060.1:c.2853_2875del	XP_011507362.1:p.Asp951GlufsTer11
XM_011509061.1:c.2775_2797del	XP_011507363.1:p.Asp925GlufsTer11
XM_011509062.1:c.2742_2764del	XP_011507364.1:p.Asp914GlufsTer11
NM_001025107.3:c.1839_1861del	NP_001020278.1:p.Asp613GlufsTer11
NM_001111.5:c.2724_2746del MANE Select	NP_001102.3:p.Asp908GlufsTer11
NM_001193495.2:c.1839_1861del	NP_001180424.1:p.Asp613GlufsTer11
NM_001365045.1:c.2751_2773del	NP_001351974.1:p.Asp917GlufsTer11
NM_001365046.1:c.1839_1861del	NP_001351975.1:p.Asp613GlufsTer11
NM_001365047.1:c.1839_1861del	NP_001351976.1:p.Asp613GlufsTer11
NM_001365048.1:c.1839_1861del	NP_001351977.1:p.Asp613GlufsTer11
NM_001365049.1:c.1761_1783del	NP_001351978.1:p.Asp587GlufsTer11
NM_015840.4:c.2646_2668del	NP_056655.3:p.Asp882GlufsTer11
NM_015841.4:c.2589_2611del	NP_056656.3:p.Asp863GlufsTer11
XM_006711113.2:c.1839_1861del	XP_006711176.1:p.Asp613GlufsTer11
XM_011509061.2:c.1761_1783del	XP_011507363.2:p.Asp587GlufsTer11
XM_024449674.1:c.2853_2875del	XP_024305442.1:p.Asp951GlufsTer11