Canonical Allele Identifier: CA342636866

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562292G>C (hg19) ; chr1:g.154589816G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589816G>C , CM000663.2:g.154589816G>C	GRCh38
NC_000001.10:g.154562292G>C , CM000663.1:g.154562292G>C	GRCh37
NC_000001.9:g.152828916G>C	NCBI36
NG_011844.1:g.43146C>G
NG_011844.2:g.46745C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2503C>G	ENSP00000497790.2:n.2503C>G
ENST00000649724.2:c.2639C>G	ENSP00000497932.2:p.Ala880Gly
ENST00000680270.2:c.2492C>G	ENSP00000505532.2:p.Ala831Gly
ENST00000681056.2:c.2261C>G	ENSP00000506234.2:p.Ala754Gly
ENST00000368471.8:c.1724C>G	ENSP00000357456.3:p.Ala575Gly
ENST00000368474.9:c.2609C>G MANE Select	ENSP00000357459.4:p.Ala870Gly
ENST00000529168.2:c.2531C>G	ENSP00000431794.2:p.Ala844Gly
ENST00000647682.2:n.2594C>G
ENST00000648231.2:c.1724C>G	ENSP00000497555.1:p.Ala575Gly
ENST00000648311.1:c.1724C>G	ENSP00000498137.1:p.Ala575Gly
ENST00000648714.2:c.*84C>G	ENSP00000497434.2:n.*84C>G
ENST00000649021.1:n.2645C>G
ENST00000649022.2:c.1724C>G	ENSP00000496896.2:p.Ala575Gly
ENST00000649042.1:c.1724C>G	ENSP00000497790.1:p.Ala575Gly
ENST00000649408.2:c.2609C>G	ENSP00000497386.2:p.Ala870Gly
ENST00000649724.1:c.1724C>G	ENSP00000497932.1:p.Ala575Gly
ENST00000649749.1:c.1724C>G	ENSP00000497210.1:p.Ala575Gly
ENST00000679375.1:c.*841C>G	ENSP00000505887.1:n.*841C>G
ENST00000679465.1:n.3062C>G
ENST00000679805.1:n.2645C>G
ENST00000679899.1:c.1667C>G	ENSP00000505996.1:p.Ala556Gly
ENST00000680270.1:c.1724C>G	ENSP00000505532.1:p.Ala575Gly
ENST00000680305.1:c.2609C>G	ENSP00000506312.1:p.Ala870Gly
ENST00000681056.1:c.1724C>G	ENSP00000506234.1:p.Ala575Gly
ENST00000681235.1:c.*2131C>G	ENSP00000506606.1:n.*2131C>G
ENST00000681429.1:n.1869C>G
ENST00000681683.1:c.1724C>G	ENSP00000506666.1:p.Ala575Gly
ENST00000681786.1:n.3062C>G
ENST00000681901.1:c.*2209C>G	ENSP00000504883.1:n.*2209C>G
ENST00000368471.7:c.1724C>G	ENSP00000357456.3:p.Ala575Gly
ENST00000368474.8:c.2609C>G	ENSP00000357459.4:p.Ala870Gly
ENST00000529168.1:c.2516C>G	ENSP00000431794.1:p.Ala839Gly
NM_001025107.2:c.1724C>G	NP_001020278.1:p.Ala575Gly
NM_001111.4:c.2609C>G	NP_001102.2:p.Ala870Gly
NM_001193495.1:c.1724C>G	NP_001180424.1:p.Ala575Gly
NM_015840.3:c.2531C>G	NP_056655.2:p.Ala844Gly
NM_015841.3:c.2474C>G	NP_056656.2:p.Ala825Gly
XM_006711109.1:c.2639C>G	XP_006711172.1:p.Ala880Gly
XM_006711111.2:c.1724C>G	XP_006711174.1:p.Ala575Gly
XM_006711112.1:c.1724C>G	XP_006711175.1:p.Ala575Gly
XM_006711113.1:c.1724C>G	XP_006711176.1:p.Ala575Gly
XM_011509060.1:c.2738C>G	XP_011507362.1:p.Ala913Gly
XM_011509061.1:c.2660C>G	XP_011507363.1:p.Ala887Gly
XM_011509062.1:c.2627C>G	XP_011507364.1:p.Ala876Gly
NM_001025107.3:c.1724C>G	NP_001020278.1:p.Ala575Gly
NM_001111.5:c.2609C>G MANE Select	NP_001102.3:p.Ala870Gly
NM_001193495.2:c.1724C>G	NP_001180424.1:p.Ala575Gly
NM_001365045.1:c.2636C>G	NP_001351974.1:p.Ala879Gly
NM_001365046.1:c.1724C>G	NP_001351975.1:p.Ala575Gly
NM_001365047.1:c.1724C>G	NP_001351976.1:p.Ala575Gly
NM_001365048.1:c.1724C>G	NP_001351977.1:p.Ala575Gly
NM_001365049.1:c.1646C>G	NP_001351978.1:p.Ala549Gly
NM_015840.4:c.2531C>G	NP_056655.3:p.Ala844Gly
NM_015841.4:c.2474C>G	NP_056656.3:p.Ala825Gly
XM_006711113.2:c.1724C>G	XP_006711176.1:p.Ala575Gly
XM_011509061.2:c.1646C>G	XP_011507363.2:p.Ala549Gly
XM_024449674.1:c.2738C>G	XP_024305442.1:p.Ala913Gly