Canonical Allele Identifier: CA342634988

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557709T>A (hg19) ; chr1:g.154585233T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585233T>A , CM000663.2:g.154585233T>A	GRCh38
NC_000001.10:g.154557709T>A , CM000663.1:g.154557709T>A	GRCh37
NC_000001.9:g.152824333T>A	NCBI36
NG_011844.1:g.47729A>T
NG_011844.2:g.51328A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3321A>T	ENSP00000497790.2:n.3321A>T
ENST00000649724.2:c.3457A>T	ENSP00000497932.2:p.Arg1153Ter
ENST00000680270.2:c.3310A>T	ENSP00000505532.2:p.Arg1104Ter
ENST00000681056.2:c.3079A>T	ENSP00000506234.2:p.Arg1027Ter
ENST00000368471.8:c.2542A>T	ENSP00000357456.3:p.Arg848Ter
ENST00000368474.9:c.3427A>T MANE Select	ENSP00000357459.4:p.Arg1143Ter
ENST00000492630.2:n.2220A>T
ENST00000529168.2:c.3349A>T	ENSP00000431794.2:p.Arg1117Ter
ENST00000647682.2:n.3412A>T
ENST00000648231.2:c.2542A>T	ENSP00000497555.1:p.Arg848Ter
ENST00000648311.1:c.2542A>T	ENSP00000498137.1:p.Arg848Ter
ENST00000648714.2:c.*902A>T	ENSP00000497434.2:n.*902A>T
ENST00000649021.1:n.4163A>T
ENST00000649022.2:c.2542A>T	ENSP00000496896.2:p.Arg848Ter
ENST00000649042.1:c.2542A>T	ENSP00000497790.1:p.Arg848Ter
ENST00000649408.2:c.*593A>T	ENSP00000497386.2:n.*593A>T
ENST00000649724.1:c.2542A>T	ENSP00000497932.1:p.Arg848Ter
ENST00000649749.1:c.2542A>T	ENSP00000497210.1:p.Arg848Ter
ENST00000679375.1:c.*1659A>T	ENSP00000505887.1:n.*1659A>T
ENST00000679465.1:n.4288A>T
ENST00000679805.1:n.4163A>T
ENST00000679899.1:c.2485A>T	ENSP00000505996.1:p.Arg829Ter
ENST00000680270.1:c.2542A>T	ENSP00000505532.1:p.Arg848Ter
ENST00000680305.1:c.3244A>T	ENSP00000506312.1:p.Arg1082Ter
ENST00000681056.1:c.2542A>T	ENSP00000506234.1:p.Arg848Ter
ENST00000681235.1:c.*2949A>T	ENSP00000506606.1:n.*2949A>T
ENST00000681429.1:n.3095A>T
ENST00000681683.1:c.2542A>T	ENSP00000506666.1:p.Arg848Ter
ENST00000681786.1:n.4288A>T
ENST00000681901.1:c.*3027A>T	ENSP00000504883.1:n.*3027A>T
ENST00000368471.7:c.2542A>T	ENSP00000357456.3:p.Arg848Ter
ENST00000368474.8:c.3427A>T	ENSP00000357459.4:p.Arg1143Ter
ENST00000492630.1:n.186A>T
ENST00000529168.1:c.3334A>T	ENSP00000431794.1:p.Arg1112Ter
NM_001025107.2:c.2542A>T	NP_001020278.1:p.Arg848Ter
NM_001111.4:c.3427A>T	NP_001102.2:p.Arg1143Ter
NM_001193495.1:c.2542A>T	NP_001180424.1:p.Arg848Ter
NM_015840.3:c.3349A>T	NP_056655.2:p.Arg1117Ter
NM_015841.3:c.3292A>T	NP_056656.2:p.Arg1098Ter
XM_006711109.1:c.3457A>T	XP_006711172.1:p.Arg1153Ter
XM_006711111.2:c.2542A>T	XP_006711174.1:p.Arg848Ter
XM_006711112.1:c.2542A>T	XP_006711175.1:p.Arg848Ter
XM_006711113.1:c.2542A>T	XP_006711176.1:p.Arg848Ter
XM_011509060.1:c.3556A>T	XP_011507362.1:p.Arg1186Ter
XM_011509061.1:c.3478A>T	XP_011507363.1:p.Arg1160Ter
XM_011509062.1:c.3445A>T	XP_011507364.1:p.Arg1149Ter
NM_001025107.3:c.2542A>T	NP_001020278.1:p.Arg848Ter
NM_001111.5:c.3427A>T MANE Select	NP_001102.3:p.Arg1143Ter
NM_001193495.2:c.2542A>T	NP_001180424.1:p.Arg848Ter
NM_001365045.1:c.3454A>T	NP_001351974.1:p.Arg1152Ter
NM_001365046.1:c.2542A>T	NP_001351975.1:p.Arg848Ter
NM_001365047.1:c.2542A>T	NP_001351976.1:p.Arg848Ter
NM_001365048.1:c.2542A>T	NP_001351977.1:p.Arg848Ter
NM_001365049.1:c.2464A>T	NP_001351978.1:p.Arg822Ter
NM_015840.4:c.3349A>T	NP_056655.3:p.Arg1117Ter
NM_015841.4:c.3292A>T	NP_056656.3:p.Arg1098Ter
XM_006711113.2:c.2542A>T	XP_006711176.1:p.Arg848Ter
XM_011509061.2:c.2464A>T	XP_011507363.2:p.Arg822Ter
XM_024449674.1:c.3556A>T	XP_024305442.1:p.Arg1186Ter