Canonical Allele Identifier: CA342634649

Gene: ADAR

Linked Data

• COSMIC: COSM5619808 ; COSM5619809
• MyVariant Identifiers: chr1:g.154557383T>C (hg19) ; chr1:g.154584907T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584907T>C , CM000663.2:g.154584907T>C	GRCh38
NC_000001.10:g.154557383T>C , CM000663.1:g.154557383T>C	GRCh37
NC_000001.9:g.152824007T>C	NCBI36
NG_011844.1:g.48055A>G
NG_011844.2:g.51654A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3474A>G	ENSP00000497790.2:n.3474A>G
ENST00000649724.2:c.3610A>G	ENSP00000497932.2:p.Thr1204Ala
ENST00000680270.2:c.3463A>G	ENSP00000505532.2:p.Thr1155Ala
ENST00000681056.2:c.3232A>G	ENSP00000506234.2:p.Thr1078Ala
ENST00000368471.8:c.2695A>G	ENSP00000357456.3:p.Thr899Ala
ENST00000368474.9:c.3580A>G MANE Select	ENSP00000357459.4:p.Thr1194Ala
ENST00000492630.2:n.2373A>G
ENST00000529168.2:c.3502A>G	ENSP00000431794.2:p.Thr1168Ala
ENST00000647682.2:n.3565A>G
ENST00000648231.2:c.2695A>G	ENSP00000497555.1:p.Thr899Ala
ENST00000648311.1:c.2695A>G	ENSP00000498137.1:p.Thr899Ala
ENST00000648714.2:c.*1055A>G	ENSP00000497434.2:n.*1055A>G
ENST00000649021.1:n.4316A>G
ENST00000649022.2:c.2695A>G	ENSP00000496896.2:p.Thr899Ala
ENST00000649042.1:c.2695A>G	ENSP00000497790.1:p.Thr899Ala
ENST00000649408.2:c.*746A>G	ENSP00000497386.2:n.*746A>G
ENST00000649724.1:c.2695A>G	ENSP00000497932.1:p.Thr899Ala
ENST00000649749.1:c.2695A>G	ENSP00000497210.1:p.Thr899Ala
ENST00000679375.1:c.*1812A>G	ENSP00000505887.1:n.*1812A>G
ENST00000679465.1:n.4441A>G
ENST00000679805.1:n.4316A>G
ENST00000679899.1:c.2638A>G	ENSP00000505996.1:p.Thr880Ala
ENST00000680270.1:c.2695A>G	ENSP00000505532.1:p.Thr899Ala
ENST00000680305.1:c.3397A>G	ENSP00000506312.1:p.Thr1133Ala
ENST00000681056.1:c.2695A>G	ENSP00000506234.1:p.Thr899Ala
ENST00000681235.1:c.*3102A>G	ENSP00000506606.1:n.*3102A>G
ENST00000681429.1:n.3248A>G
ENST00000681683.1:c.2695A>G	ENSP00000506666.1:p.Thr899Ala
ENST00000681786.1:n.4441A>G
ENST00000681901.1:c.*3180A>G	ENSP00000504883.1:n.*3180A>G
ENST00000368471.7:c.2695A>G	ENSP00000357456.3:p.Thr899Ala
ENST00000368474.8:c.3580A>G	ENSP00000357459.4:p.Thr1194Ala
ENST00000492630.1:n.339A>G
ENST00000529168.1:c.3487A>G	ENSP00000431794.1:p.Thr1163Ala
NM_001025107.2:c.2695A>G	NP_001020278.1:p.Thr899Ala
NM_001111.4:c.3580A>G	NP_001102.2:p.Thr1194Ala
NM_001193495.1:c.2695A>G	NP_001180424.1:p.Thr899Ala
NM_015840.3:c.3502A>G	NP_056655.2:p.Thr1168Ala
NM_015841.3:c.3445A>G	NP_056656.2:p.Thr1149Ala
XM_006711109.1:c.3610A>G	XP_006711172.1:p.Thr1204Ala
XM_006711111.2:c.2695A>G	XP_006711174.1:p.Thr899Ala
XM_006711112.1:c.2695A>G	XP_006711175.1:p.Thr899Ala
XM_006711113.1:c.2695A>G	XP_006711176.1:p.Thr899Ala
XM_011509060.1:c.3709A>G	XP_011507362.1:p.Thr1237Ala
XM_011509061.1:c.3631A>G	XP_011507363.1:p.Thr1211Ala
XM_011509062.1:c.3598A>G	XP_011507364.1:p.Thr1200Ala
NM_001025107.3:c.2695A>G	NP_001020278.1:p.Thr899Ala
NM_001111.5:c.3580A>G MANE Select	NP_001102.3:p.Thr1194Ala
NM_001193495.2:c.2695A>G	NP_001180424.1:p.Thr899Ala
NM_001365045.1:c.3607A>G	NP_001351974.1:p.Thr1203Ala
NM_001365046.1:c.2695A>G	NP_001351975.1:p.Thr899Ala
NM_001365047.1:c.2695A>G	NP_001351976.1:p.Thr899Ala
NM_001365048.1:c.2695A>G	NP_001351977.1:p.Thr899Ala
NM_001365049.1:c.2617A>G	NP_001351978.1:p.Thr873Ala
NM_015840.4:c.3502A>G	NP_056655.3:p.Thr1168Ala
NM_015841.4:c.3445A>G	NP_056656.3:p.Thr1149Ala
XM_006711113.2:c.2695A>G	XP_006711176.1:p.Thr899Ala
XM_011509061.2:c.2617A>G	XP_011507363.2:p.Thr873Ala
XM_024449674.1:c.3709A>G	XP_024305442.1:p.Thr1237Ala