Canonical Allele Identifier: CA342636833

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562275T>G (hg19) ; chr1:g.154589799T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589799T>G , CM000663.2:g.154589799T>G	GRCh38
NC_000001.10:g.154562275T>G , CM000663.1:g.154562275T>G	GRCh37
NC_000001.9:g.152828899T>G	NCBI36
NG_011844.1:g.43163A>C
NG_011844.2:g.46762A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2520A>C	ENSP00000497790.2:n.2520A>C
ENST00000649724.2:c.2656A>C	ENSP00000497932.2:p.Lys886Gln
ENST00000680270.2:c.2509A>C	ENSP00000505532.2:p.Lys837Gln
ENST00000681056.2:c.2278A>C	ENSP00000506234.2:p.Lys760Gln
ENST00000368471.8:c.1741A>C	ENSP00000357456.3:p.Lys581Gln
ENST00000368474.9:c.2626A>C MANE Select	ENSP00000357459.4:p.Lys876Gln
ENST00000529168.2:c.2548A>C	ENSP00000431794.2:p.Lys850Gln
ENST00000647682.2:n.2611A>C
ENST00000648231.2:c.1741A>C	ENSP00000497555.1:p.Lys581Gln
ENST00000648311.1:c.1741A>C	ENSP00000498137.1:p.Lys581Gln
ENST00000648714.2:c.*101A>C	ENSP00000497434.2:n.*101A>C
ENST00000649021.1:n.2662A>C
ENST00000649022.2:c.1741A>C	ENSP00000496896.2:p.Lys581Gln
ENST00000649042.1:c.1741A>C	ENSP00000497790.1:p.Lys581Gln
ENST00000649408.2:c.2626A>C	ENSP00000497386.2:p.Lys876Gln
ENST00000649724.1:c.1741A>C	ENSP00000497932.1:p.Lys581Gln
ENST00000649749.1:c.1741A>C	ENSP00000497210.1:p.Lys581Gln
ENST00000679375.1:c.*858A>C	ENSP00000505887.1:n.*858A>C
ENST00000679465.1:n.3079A>C
ENST00000679805.1:n.2662A>C
ENST00000679899.1:c.1684A>C	ENSP00000505996.1:p.Lys562Gln
ENST00000680270.1:c.1741A>C	ENSP00000505532.1:p.Lys581Gln
ENST00000680305.1:c.2626A>C	ENSP00000506312.1:p.Lys876Gln
ENST00000681056.1:c.1741A>C	ENSP00000506234.1:p.Lys581Gln
ENST00000681235.1:c.*2148A>C	ENSP00000506606.1:n.*2148A>C
ENST00000681429.1:n.1886A>C
ENST00000681683.1:c.1741A>C	ENSP00000506666.1:p.Lys581Gln
ENST00000681786.1:n.3079A>C
ENST00000681901.1:c.*2226A>C	ENSP00000504883.1:n.*2226A>C
ENST00000368471.7:c.1741A>C	ENSP00000357456.3:p.Lys581Gln
ENST00000368474.8:c.2626A>C	ENSP00000357459.4:p.Lys876Gln
ENST00000529168.1:c.2533A>C	ENSP00000431794.1:p.Lys845Gln
NM_001025107.2:c.1741A>C	NP_001020278.1:p.Lys581Gln
NM_001111.4:c.2626A>C	NP_001102.2:p.Lys876Gln
NM_001193495.1:c.1741A>C	NP_001180424.1:p.Lys581Gln
NM_015840.3:c.2548A>C	NP_056655.2:p.Lys850Gln
NM_015841.3:c.2491A>C	NP_056656.2:p.Lys831Gln
XM_006711109.1:c.2656A>C	XP_006711172.1:p.Lys886Gln
XM_006711111.2:c.1741A>C	XP_006711174.1:p.Lys581Gln
XM_006711112.1:c.1741A>C	XP_006711175.1:p.Lys581Gln
XM_006711113.1:c.1741A>C	XP_006711176.1:p.Lys581Gln
XM_011509060.1:c.2755A>C	XP_011507362.1:p.Lys919Gln
XM_011509061.1:c.2677A>C	XP_011507363.1:p.Lys893Gln
XM_011509062.1:c.2644A>C	XP_011507364.1:p.Lys882Gln
NM_001025107.3:c.1741A>C	NP_001020278.1:p.Lys581Gln
NM_001111.5:c.2626A>C MANE Select	NP_001102.3:p.Lys876Gln
NM_001193495.2:c.1741A>C	NP_001180424.1:p.Lys581Gln
NM_001365045.1:c.2653A>C	NP_001351974.1:p.Lys885Gln
NM_001365046.1:c.1741A>C	NP_001351975.1:p.Lys581Gln
NM_001365047.1:c.1741A>C	NP_001351976.1:p.Lys581Gln
NM_001365048.1:c.1741A>C	NP_001351977.1:p.Lys581Gln
NM_001365049.1:c.1663A>C	NP_001351978.1:p.Lys555Gln
NM_015840.4:c.2548A>C	NP_056655.3:p.Lys850Gln
NM_015841.4:c.2491A>C	NP_056656.3:p.Lys831Gln
XM_006711113.2:c.1741A>C	XP_006711176.1:p.Lys581Gln
XM_011509061.2:c.1663A>C	XP_011507363.2:p.Lys555Gln
XM_024449674.1:c.2755A>C	XP_024305442.1:p.Lys919Gln