Canonical Allele Identifier: CA342635677

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154586258C>T , CM000663.2:g.154586258C>T	GRCh38
NC_000001.10:g.154558734C>T , CM000663.1:g.154558734C>T	GRCh37
NC_000001.9:g.152825358C>T	NCBI36
NG_011844.1:g.46704G>A
NG_011844.2:g.50303G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.3125G>A MANE Select	NP_001102.3:p.Arg1042His
ENST00000368474.9:c.3125G>A MANE Select	ENSP00000357459.4:p.Arg1042His
NM_001025107.2:c.2240G>A	NP_001020278.1:p.Arg747His
NM_001025107.3:c.2240G>A	NP_001020278.1:p.Arg747His
NM_001111.4:c.3125G>A	NP_001102.2:p.Arg1042His
NM_001193495.1:c.2240G>A	NP_001180424.1:p.Arg747His
NM_001193495.2:c.2240G>A	NP_001180424.1:p.Arg747His
NM_001365045.1:c.3152G>A	NP_001351974.1:p.Arg1051His
NM_001365046.1:c.2240G>A	NP_001351975.1:p.Arg747His
NM_001365047.1:c.2240G>A	NP_001351976.1:p.Arg747His
NM_001365048.1:c.2240G>A	NP_001351977.1:p.Arg747His
NM_001365049.1:c.2162G>A	NP_001351978.1:p.Arg721His
NM_015840.3:c.3047G>A	NP_056655.2:p.Arg1016His
NM_015840.4:c.3047G>A	NP_056655.3:p.Arg1016His
NM_015841.3:c.2990G>A	NP_056656.2:p.Arg997His
NM_015841.4:c.2990G>A	NP_056656.3:p.Arg997His
ENST00000368471.7:c.2240G>A	ENSP00000357456.3:p.Arg747His
ENST00000368471.8:c.2240G>A	ENSP00000357456.3:p.Arg747His
ENST00000368474.8:c.3125G>A	ENSP00000357459.4:p.Arg1042His
ENST00000492630.2:n.1510G>A
ENST00000529168.1:c.3032G>A	ENSP00000431794.1:p.Arg1011His
ENST00000529168.2:c.3047G>A	ENSP00000431794.2:p.Arg1016His
ENST00000530954.1:n.262G>A
ENST00000534279.1:n.584G>A
ENST00000647682.2:n.3110G>A
ENST00000648231.2:c.2240G>A	ENSP00000497555.1:p.Arg747His
ENST00000648311.1:c.2240G>A	ENSP00000498137.1:p.Arg747His
ENST00000648714.2:c.*600G>A	ENSP00000497434.2:n.*600G>A
ENST00000649021.1:n.3453G>A
ENST00000649022.2:c.2240G>A	ENSP00000496896.2:p.Arg747His
ENST00000649042.1:c.2240G>A	ENSP00000497790.1:p.Arg747His
ENST00000649042.2:c.3019G>A	ENSP00000497790.2:n.3019G>A
ENST00000649408.2:c.*291G>A	ENSP00000497386.2:n.*291G>A
ENST00000649724.1:c.2240G>A	ENSP00000497932.1:p.Arg747His
ENST00000649724.2:c.3155G>A	ENSP00000497932.2:p.Arg1052His
ENST00000649749.1:c.2240G>A	ENSP00000497210.1:p.Arg747His
ENST00000679375.1:c.*1357G>A	ENSP00000505887.1:n.*1357G>A
ENST00000679465.1:n.3578G>A
ENST00000679805.1:n.3453G>A
ENST00000679899.1:c.2183G>A	ENSP00000505996.1:p.Arg728His
ENST00000680270.1:c.2240G>A	ENSP00000505532.1:p.Arg747His
ENST00000680270.2:c.3008G>A	ENSP00000505532.2:p.Arg1003His
ENST00000680305.1:c.3020-393G>A	ENSP00000506312.1:n.3020-393G>A
ENST00000681056.1:c.2240G>A	ENSP00000506234.1:p.Arg747His
ENST00000681056.2:c.2777G>A	ENSP00000506234.2:p.Arg926His
ENST00000681235.1:c.*2647G>A	ENSP00000506606.1:n.*2647G>A
ENST00000681429.1:n.2385G>A
ENST00000681683.1:c.2240G>A	ENSP00000506666.1:p.Arg747His
ENST00000681786.1:n.3578G>A
ENST00000681901.1:c.*2725G>A	ENSP00000504883.1:n.*2725G>A
XM_006711109.1:c.3155G>A	XP_006711172.1:p.Arg1052His
XM_006711111.2:c.2240G>A	XP_006711174.1:p.Arg747His
XM_006711112.1:c.2240G>A	XP_006711175.1:p.Arg747His
XM_006711113.1:c.2240G>A	XP_006711176.1:p.Arg747His
XM_006711113.2:c.2240G>A	XP_006711176.1:p.Arg747His
XM_011509060.1:c.3254G>A	XP_011507362.1:p.Arg1085His
XM_011509061.1:c.3176G>A	XP_011507363.1:p.Arg1059His
XM_011509061.2:c.2162G>A	XP_011507363.2:p.Arg721His
XM_011509062.1:c.3143G>A	XP_011507364.1:p.Arg1048His
XM_024449674.1:c.3254G>A	XP_024305442.1:p.Arg1085His