Canonical Allele Identifier: CA342634846

Gene: ADAR

Linked Data

• gnomAD v4: 1-154584997-G-T
• MyVariant Identifiers: chr1:g.154557473G>T (hg19) ; chr1:g.154584997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584997G>T , CM000663.2:g.154584997G>T	GRCh38
NC_000001.10:g.154557473G>T , CM000663.1:g.154557473G>T	GRCh37
NC_000001.9:g.152824097G>T	NCBI36
NG_011844.1:g.47965C>A
NG_011844.2:g.51564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3384C>A	ENSP00000497790.2:n.3384C>A
ENST00000649724.2:c.3520C>A	ENSP00000497932.2:p.Leu1174Ile
ENST00000680270.2:c.3373C>A	ENSP00000505532.2:p.Leu1125Ile
ENST00000681056.2:c.3142C>A	ENSP00000506234.2:p.Leu1048Ile
ENST00000368471.8:c.2605C>A	ENSP00000357456.3:p.Leu869Ile
ENST00000368474.9:c.3490C>A MANE Select	ENSP00000357459.4:p.Leu1164Ile
ENST00000492630.2:n.2283C>A
ENST00000529168.2:c.3412C>A	ENSP00000431794.2:p.Leu1138Ile
ENST00000647682.2:n.3475C>A
ENST00000648231.2:c.2605C>A	ENSP00000497555.1:p.Leu869Ile
ENST00000648311.1:c.2605C>A	ENSP00000498137.1:p.Leu869Ile
ENST00000648714.2:c.*965C>A	ENSP00000497434.2:n.*965C>A
ENST00000649021.1:n.4226C>A
ENST00000649022.2:c.2605C>A	ENSP00000496896.2:p.Leu869Ile
ENST00000649042.1:c.2605C>A	ENSP00000497790.1:p.Leu869Ile
ENST00000649408.2:c.*656C>A	ENSP00000497386.2:n.*656C>A
ENST00000649724.1:c.2605C>A	ENSP00000497932.1:p.Leu869Ile
ENST00000649749.1:c.2605C>A	ENSP00000497210.1:p.Leu869Ile
ENST00000679375.1:c.*1722C>A	ENSP00000505887.1:n.*1722C>A
ENST00000679465.1:n.4351C>A
ENST00000679805.1:n.4226C>A
ENST00000679899.1:c.2548C>A	ENSP00000505996.1:p.Leu850Ile
ENST00000680270.1:c.2605C>A	ENSP00000505532.1:p.Leu869Ile
ENST00000680305.1:c.3307C>A	ENSP00000506312.1:p.Leu1103Ile
ENST00000681056.1:c.2605C>A	ENSP00000506234.1:p.Leu869Ile
ENST00000681235.1:c.*3012C>A	ENSP00000506606.1:n.*3012C>A
ENST00000681429.1:n.3158C>A
ENST00000681683.1:c.2605C>A	ENSP00000506666.1:p.Leu869Ile
ENST00000681786.1:n.4351C>A
ENST00000681901.1:c.*3090C>A	ENSP00000504883.1:n.*3090C>A
ENST00000368471.7:c.2605C>A	ENSP00000357456.3:p.Leu869Ile
ENST00000368474.8:c.3490C>A	ENSP00000357459.4:p.Leu1164Ile
ENST00000492630.1:n.249C>A
ENST00000529168.1:c.3397C>A	ENSP00000431794.1:p.Leu1133Ile
NM_001025107.2:c.2605C>A	NP_001020278.1:p.Leu869Ile
NM_001111.4:c.3490C>A	NP_001102.2:p.Leu1164Ile
NM_001193495.1:c.2605C>A	NP_001180424.1:p.Leu869Ile
NM_015840.3:c.3412C>A	NP_056655.2:p.Leu1138Ile
NM_015841.3:c.3355C>A	NP_056656.2:p.Leu1119Ile
XM_006711109.1:c.3520C>A	XP_006711172.1:p.Leu1174Ile
XM_006711111.2:c.2605C>A	XP_006711174.1:p.Leu869Ile
XM_006711112.1:c.2605C>A	XP_006711175.1:p.Leu869Ile
XM_006711113.1:c.2605C>A	XP_006711176.1:p.Leu869Ile
XM_011509060.1:c.3619C>A	XP_011507362.1:p.Leu1207Ile
XM_011509061.1:c.3541C>A	XP_011507363.1:p.Leu1181Ile
XM_011509062.1:c.3508C>A	XP_011507364.1:p.Leu1170Ile
NM_001025107.3:c.2605C>A	NP_001020278.1:p.Leu869Ile
NM_001111.5:c.3490C>A MANE Select	NP_001102.3:p.Leu1164Ile
NM_001193495.2:c.2605C>A	NP_001180424.1:p.Leu869Ile
NM_001365045.1:c.3517C>A	NP_001351974.1:p.Leu1173Ile
NM_001365046.1:c.2605C>A	NP_001351975.1:p.Leu869Ile
NM_001365047.1:c.2605C>A	NP_001351976.1:p.Leu869Ile
NM_001365048.1:c.2605C>A	NP_001351977.1:p.Leu869Ile
NM_001365049.1:c.2527C>A	NP_001351978.1:p.Leu843Ile
NM_015840.4:c.3412C>A	NP_056655.3:p.Leu1138Ile
NM_015841.4:c.3355C>A	NP_056656.3:p.Leu1119Ile
XM_006711113.2:c.2605C>A	XP_006711176.1:p.Leu869Ile
XM_011509061.2:c.2527C>A	XP_011507363.2:p.Leu843Ile
XM_024449674.1:c.3619C>A	XP_024305442.1:p.Leu1207Ile