Canonical Allele Identifier: CA342634429

Gene: ADAR

Linked Data

• gnomAD v4: 1-154584817-A-C
• MyVariant Identifiers: chr1:g.154557293A>C (hg19) ; chr1:g.154584817A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584817A>C , CM000663.2:g.154584817A>C	GRCh38
NC_000001.10:g.154557293A>C , CM000663.1:g.154557293A>C	GRCh37
NC_000001.9:g.152823917A>C	NCBI36
NG_011844.1:g.48145T>G
NG_011844.2:g.51744T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3564T>G	ENSP00000497790.2:n.3564T>G
ENST00000649724.2:c.3700T>G	ENSP00000497932.2:p.Cys1234Gly
ENST00000680270.2:c.3553T>G	ENSP00000505532.2:p.Cys1185Gly
ENST00000681056.2:c.3322T>G	ENSP00000506234.2:p.Cys1108Gly
ENST00000368471.8:c.2785T>G	ENSP00000357456.3:p.Cys929Gly
ENST00000368474.9:c.3670T>G MANE Select	ENSP00000357459.4:p.Cys1224Gly
ENST00000492630.2:n.2463T>G
ENST00000529168.2:c.3592T>G	ENSP00000431794.2:p.Cys1198Gly
ENST00000647682.2:n.3655T>G
ENST00000648231.2:c.2785T>G	ENSP00000497555.1:p.Cys929Gly
ENST00000648311.1:c.2785T>G	ENSP00000498137.1:p.Cys929Gly
ENST00000648714.2:c.*1145T>G	ENSP00000497434.2:n.*1145T>G
ENST00000649021.1:n.4406T>G
ENST00000649022.2:c.2785T>G	ENSP00000496896.2:p.Cys929Gly
ENST00000649042.1:c.2785T>G	ENSP00000497790.1:p.Cys929Gly
ENST00000649408.2:c.*836T>G	ENSP00000497386.2:n.*836T>G
ENST00000649724.1:c.2785T>G	ENSP00000497932.1:p.Cys929Gly
ENST00000649749.1:c.2785T>G	ENSP00000497210.1:p.Cys929Gly
ENST00000679375.1:c.*1902T>G	ENSP00000505887.1:n.*1902T>G
ENST00000679465.1:n.4531T>G
ENST00000679805.1:n.4406T>G
ENST00000679899.1:c.2728T>G	ENSP00000505996.1:p.Cys910Gly
ENST00000680270.1:c.2785T>G	ENSP00000505532.1:p.Cys929Gly
ENST00000680305.1:c.3487T>G	ENSP00000506312.1:p.Cys1163Gly
ENST00000681056.1:c.2785T>G	ENSP00000506234.1:p.Cys929Gly
ENST00000681235.1:c.*3192T>G	ENSP00000506606.1:n.*3192T>G
ENST00000681429.1:n.3338T>G
ENST00000681683.1:c.2785T>G	ENSP00000506666.1:p.Cys929Gly
ENST00000681786.1:n.4531T>G
ENST00000681901.1:c.*3270T>G	ENSP00000504883.1:n.*3270T>G
ENST00000368471.7:c.2785T>G	ENSP00000357456.3:p.Cys929Gly
ENST00000368474.8:c.3670T>G	ENSP00000357459.4:p.Cys1224Gly
ENST00000492630.1:n.429T>G
ENST00000529168.1:c.3577T>G	ENSP00000431794.1:p.Cys1193Gly
NM_001025107.2:c.2785T>G	NP_001020278.1:p.Cys929Gly
NM_001111.4:c.3670T>G	NP_001102.2:p.Cys1224Gly
NM_001193495.1:c.2785T>G	NP_001180424.1:p.Cys929Gly
NM_015840.3:c.3592T>G	NP_056655.2:p.Cys1198Gly
NM_015841.3:c.3535T>G	NP_056656.2:p.Cys1179Gly
XM_006711109.1:c.3700T>G	XP_006711172.1:p.Cys1234Gly
XM_006711111.2:c.2785T>G	XP_006711174.1:p.Cys929Gly
XM_006711112.1:c.2785T>G	XP_006711175.1:p.Cys929Gly
XM_006711113.1:c.2785T>G	XP_006711176.1:p.Cys929Gly
XM_011509060.1:c.3799T>G	XP_011507362.1:p.Cys1267Gly
XM_011509061.1:c.3721T>G	XP_011507363.1:p.Cys1241Gly
XM_011509062.1:c.3688T>G	XP_011507364.1:p.Cys1230Gly
NM_001025107.3:c.2785T>G	NP_001020278.1:p.Cys929Gly
NM_001111.5:c.3670T>G MANE Select	NP_001102.3:p.Cys1224Gly
NM_001193495.2:c.2785T>G	NP_001180424.1:p.Cys929Gly
NM_001365045.1:c.3697T>G	NP_001351974.1:p.Cys1233Gly
NM_001365046.1:c.2785T>G	NP_001351975.1:p.Cys929Gly
NM_001365047.1:c.2785T>G	NP_001351976.1:p.Cys929Gly
NM_001365048.1:c.2785T>G	NP_001351977.1:p.Cys929Gly
NM_001365049.1:c.2707T>G	NP_001351978.1:p.Cys903Gly
NM_015840.4:c.3592T>G	NP_056655.3:p.Cys1198Gly
NM_015841.4:c.3535T>G	NP_056656.3:p.Cys1179Gly
XM_006711113.2:c.2785T>G	XP_006711176.1:p.Cys929Gly
XM_011509061.2:c.2707T>G	XP_011507363.2:p.Cys903Gly
XM_024449674.1:c.3799T>G	XP_024305442.1:p.Cys1267Gly