Canonical Allele Identifier: CA342634440

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557298T>C (hg19) ; chr1:g.154584822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584822T>C , CM000663.2:g.154584822T>C	GRCh38
NC_000001.10:g.154557298T>C , CM000663.1:g.154557298T>C	GRCh37
NC_000001.9:g.152823922T>C	NCBI36
NG_011844.1:g.48140A>G
NG_011844.2:g.51739A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3559A>G	ENSP00000497790.2:n.3559A>G
ENST00000649724.2:c.3695A>G	ENSP00000497932.2:p.Tyr1232Cys
ENST00000680270.2:c.3548A>G	ENSP00000505532.2:p.Tyr1183Cys
ENST00000681056.2:c.3317A>G	ENSP00000506234.2:p.Tyr1106Cys
ENST00000368471.8:c.2780A>G	ENSP00000357456.3:p.Tyr927Cys
ENST00000368474.9:c.3665A>G MANE Select	ENSP00000357459.4:p.Tyr1222Cys
ENST00000492630.2:n.2458A>G
ENST00000529168.2:c.3587A>G	ENSP00000431794.2:p.Tyr1196Cys
ENST00000647682.2:n.3650A>G
ENST00000648231.2:c.2780A>G	ENSP00000497555.1:p.Tyr927Cys
ENST00000648311.1:c.2780A>G	ENSP00000498137.1:p.Tyr927Cys
ENST00000648714.2:c.*1140A>G	ENSP00000497434.2:n.*1140A>G
ENST00000649021.1:n.4401A>G
ENST00000649022.2:c.2780A>G	ENSP00000496896.2:p.Tyr927Cys
ENST00000649042.1:c.2780A>G	ENSP00000497790.1:p.Tyr927Cys
ENST00000649408.2:c.*831A>G	ENSP00000497386.2:n.*831A>G
ENST00000649724.1:c.2780A>G	ENSP00000497932.1:p.Tyr927Cys
ENST00000649749.1:c.2780A>G	ENSP00000497210.1:p.Tyr927Cys
ENST00000679375.1:c.*1897A>G	ENSP00000505887.1:n.*1897A>G
ENST00000679465.1:n.4526A>G
ENST00000679805.1:n.4401A>G
ENST00000679899.1:c.2723A>G	ENSP00000505996.1:p.Tyr908Cys
ENST00000680270.1:c.2780A>G	ENSP00000505532.1:p.Tyr927Cys
ENST00000680305.1:c.3482A>G	ENSP00000506312.1:p.Tyr1161Cys
ENST00000681056.1:c.2780A>G	ENSP00000506234.1:p.Tyr927Cys
ENST00000681235.1:c.*3187A>G	ENSP00000506606.1:n.*3187A>G
ENST00000681429.1:n.3333A>G
ENST00000681683.1:c.2780A>G	ENSP00000506666.1:p.Tyr927Cys
ENST00000681786.1:n.4526A>G
ENST00000681901.1:c.*3265A>G	ENSP00000504883.1:n.*3265A>G
ENST00000368471.7:c.2780A>G	ENSP00000357456.3:p.Tyr927Cys
ENST00000368474.8:c.3665A>G	ENSP00000357459.4:p.Tyr1222Cys
ENST00000492630.1:n.424A>G
ENST00000529168.1:c.3572A>G	ENSP00000431794.1:p.Tyr1191Cys
NM_001025107.2:c.2780A>G	NP_001020278.1:p.Tyr927Cys
NM_001111.4:c.3665A>G	NP_001102.2:p.Tyr1222Cys
NM_001193495.1:c.2780A>G	NP_001180424.1:p.Tyr927Cys
NM_015840.3:c.3587A>G	NP_056655.2:p.Tyr1196Cys
NM_015841.3:c.3530A>G	NP_056656.2:p.Tyr1177Cys
XM_006711109.1:c.3695A>G	XP_006711172.1:p.Tyr1232Cys
XM_006711111.2:c.2780A>G	XP_006711174.1:p.Tyr927Cys
XM_006711112.1:c.2780A>G	XP_006711175.1:p.Tyr927Cys
XM_006711113.1:c.2780A>G	XP_006711176.1:p.Tyr927Cys
XM_011509060.1:c.3794A>G	XP_011507362.1:p.Tyr1265Cys
XM_011509061.1:c.3716A>G	XP_011507363.1:p.Tyr1239Cys
XM_011509062.1:c.3683A>G	XP_011507364.1:p.Tyr1228Cys
NM_001025107.3:c.2780A>G	NP_001020278.1:p.Tyr927Cys
NM_001111.5:c.3665A>G MANE Select	NP_001102.3:p.Tyr1222Cys
NM_001193495.2:c.2780A>G	NP_001180424.1:p.Tyr927Cys
NM_001365045.1:c.3692A>G	NP_001351974.1:p.Tyr1231Cys
NM_001365046.1:c.2780A>G	NP_001351975.1:p.Tyr927Cys
NM_001365047.1:c.2780A>G	NP_001351976.1:p.Tyr927Cys
NM_001365048.1:c.2780A>G	NP_001351977.1:p.Tyr927Cys
NM_001365049.1:c.2702A>G	NP_001351978.1:p.Tyr901Cys
NM_015840.4:c.3587A>G	NP_056655.3:p.Tyr1196Cys
NM_015841.4:c.3530A>G	NP_056656.3:p.Tyr1177Cys
XM_006711113.2:c.2780A>G	XP_006711176.1:p.Tyr927Cys
XM_011509061.2:c.2702A>G	XP_011507363.2:p.Tyr901Cys
XM_024449674.1:c.3794A>G	XP_024305442.1:p.Tyr1265Cys