Canonical Allele Identifier: CA342600747

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602017C>G , CM000663.2:g.154602017C>G	GRCh38
NC_000001.10:g.154574493C>G , CM000663.1:g.154574493C>G	GRCh37
NC_000001.9:g.152841117C>G	NCBI36
NG_011844.1:g.30945G>C
NG_011844.2:g.34544G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.625G>C MANE Select	NP_001102.3:p.Gly209Arg
ENST00000368474.9:c.625G>C MANE Select	ENSP00000357459.4:p.Gly209Arg
NM_001025107.2:c.-261G>C	NP_001020278.1:n.-261G>C
NM_001025107.3:c.-261G>C	NP_001020278.1:n.-261G>C
NM_001111.4:c.625G>C	NP_001102.2:p.Gly209Arg
NM_001193495.1:c.-261G>C	NP_001180424.1:n.-261G>C
NM_001193495.2:c.-261G>C	NP_001180424.1:n.-261G>C
NM_001365045.1:c.652G>C	NP_001351974.1:p.Gly218Arg
NM_001365046.1:c.-261G>C	NP_001351975.1:n.-261G>C
NM_001365047.1:c.-261G>C	NP_001351976.1:n.-261G>C
NM_001365048.1:c.-261G>C	NP_001351977.1:n.-261G>C
NM_001365049.1:c.-261G>C	NP_001351978.1:n.-261G>C
NM_015840.3:c.625G>C	NP_056655.2:p.Gly209Arg
NM_015840.4:c.625G>C	NP_056655.3:p.Gly209Arg
NM_015841.3:c.625G>C	NP_056656.2:p.Gly209Arg
NM_015841.4:c.625G>C	NP_056656.3:p.Gly209Arg
ENST00000368471.7:c.-261G>C	ENSP00000357456.3:n.-261G>C
ENST00000368471.8:c.-261G>C	ENSP00000357456.3:n.-261G>C
ENST00000368474.8:c.625G>C	ENSP00000357459.4:p.Gly209Arg
ENST00000463920.5:n.507G>C
ENST00000529168.1:c.610G>C	ENSP00000431794.1:p.Gly204Arg
ENST00000529168.2:c.625G>C	ENSP00000431794.2:p.Gly209Arg
ENST00000647682.2:n.355G>C
ENST00000648231.2:c.-261G>C	ENSP00000497555.1:n.-261G>C
ENST00000648311.1:c.-261G>C	ENSP00000498137.1:n.-261G>C
ENST00000648714.2:c.625G>C	ENSP00000497434.2:p.Gly209Arg
ENST00000648871.1:c.-261G>C	ENSP00000497793.1:n.-261G>C
ENST00000649021.1:n.661G>C
ENST00000649022.2:c.-261G>C	ENSP00000496896.2:n.-261G>C
ENST00000649042.1:c.-261G>C	ENSP00000497790.1:n.-261G>C
ENST00000649042.2:c.519G>C	ENSP00000497790.2:n.519G>C
ENST00000649408.2:c.625G>C	ENSP00000497386.2:p.Gly209Arg
ENST00000649724.1:c.-261G>C	ENSP00000497932.1:n.-261G>C
ENST00000649724.2:c.655G>C	ENSP00000497932.2:p.Gly219Arg
ENST00000649749.1:c.-261G>C	ENSP00000497210.1:n.-261G>C
ENST00000679375.1:c.-261G>C	ENSP00000505887.1:n.-261G>C
ENST00000679465.1:n.823G>C
ENST00000679805.1:n.661G>C
ENST00000679899.1:c.-261G>C	ENSP00000505996.1:n.-261G>C
ENST00000680270.1:c.-133+19G>C	ENSP00000505532.1:n.-133+19G>C
ENST00000680270.2:c.636+19G>C	ENSP00000505532.2:n.636+19G>C
ENST00000680305.1:c.625G>C	ENSP00000506312.1:p.Gly209Arg
ENST00000680472.1:n.664G>C
ENST00000681056.1:c.-261G>C	ENSP00000506234.1:n.-261G>C
ENST00000681056.2:c.277G>C	ENSP00000506234.2:p.Gly93Arg
ENST00000681235.1:c.*225G>C	ENSP00000506606.1:n.*225G>C
ENST00000681683.1:c.-261G>C	ENSP00000506666.1:n.-261G>C
ENST00000681786.1:n.823G>C
ENST00000681901.1:c.*225G>C	ENSP00000504883.1:n.*225G>C
XM_006711109.1:c.655G>C	XP_006711172.1:p.Gly219Arg
XM_006711111.2:c.-261G>C	XP_006711174.1:n.-261G>C
XM_006711112.1:c.-261G>C	XP_006711175.1:n.-261G>C
XM_006711113.1:c.-261G>C	XP_006711176.1:n.-261G>C
XM_006711113.2:c.-261G>C	XP_006711176.1:n.-261G>C
XM_011509060.1:c.754G>C	XP_011507362.1:p.Gly252Arg
XM_011509061.1:c.754G>C	XP_011507363.1:p.Gly252Arg
XM_011509061.2:c.-261G>C	XP_011507363.2:n.-261G>C
XM_011509062.1:c.643G>C	XP_011507364.1:p.Gly215Arg
XM_024449674.1:c.754G>C	XP_024305442.1:p.Gly252Arg