Canonical Allele Identifier: CA342634970

Gene: ADAR

Linked Data

• gnomAD v4: 1-154585224-C-A
• MyVariant Identifiers: chr1:g.154557700C>A (hg19) ; chr1:g.154585224C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585224C>A , CM000663.2:g.154585224C>A	GRCh38
NC_000001.10:g.154557700C>A , CM000663.1:g.154557700C>A	GRCh37
NC_000001.9:g.152824324C>A	NCBI36
NG_011844.1:g.47738G>T
NG_011844.2:g.51337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3330G>T	ENSP00000497790.2:n.3330G>T
ENST00000649724.2:c.3466G>T	ENSP00000497932.2:p.Val1156Leu
ENST00000680270.2:c.3319G>T	ENSP00000505532.2:p.Val1107Leu
ENST00000681056.2:c.3088G>T	ENSP00000506234.2:p.Val1030Leu
ENST00000368471.8:c.2551G>T	ENSP00000357456.3:p.Val851Leu
ENST00000368474.9:c.3436G>T MANE Select	ENSP00000357459.4:p.Val1146Leu
ENST00000492630.2:n.2229G>T
ENST00000529168.2:c.3358G>T	ENSP00000431794.2:p.Val1120Leu
ENST00000647682.2:n.3421G>T
ENST00000648231.2:c.2551G>T	ENSP00000497555.1:p.Val851Leu
ENST00000648311.1:c.2551G>T	ENSP00000498137.1:p.Val851Leu
ENST00000648714.2:c.*911G>T	ENSP00000497434.2:n.*911G>T
ENST00000649021.1:n.4172G>T
ENST00000649022.2:c.2551G>T	ENSP00000496896.2:p.Val851Leu
ENST00000649042.1:c.2551G>T	ENSP00000497790.1:p.Val851Leu
ENST00000649408.2:c.*602G>T	ENSP00000497386.2:n.*602G>T
ENST00000649724.1:c.2551G>T	ENSP00000497932.1:p.Val851Leu
ENST00000649749.1:c.2551G>T	ENSP00000497210.1:p.Val851Leu
ENST00000679375.1:c.*1668G>T	ENSP00000505887.1:n.*1668G>T
ENST00000679465.1:n.4297G>T
ENST00000679805.1:n.4172G>T
ENST00000679899.1:c.2494G>T	ENSP00000505996.1:p.Val832Leu
ENST00000680270.1:c.2551G>T	ENSP00000505532.1:p.Val851Leu
ENST00000680305.1:c.3253G>T	ENSP00000506312.1:p.Val1085Leu
ENST00000681056.1:c.2551G>T	ENSP00000506234.1:p.Val851Leu
ENST00000681235.1:c.*2958G>T	ENSP00000506606.1:n.*2958G>T
ENST00000681429.1:n.3104G>T
ENST00000681683.1:c.2551G>T	ENSP00000506666.1:p.Val851Leu
ENST00000681786.1:n.4297G>T
ENST00000681901.1:c.*3036G>T	ENSP00000504883.1:n.*3036G>T
ENST00000368471.7:c.2551G>T	ENSP00000357456.3:p.Val851Leu
ENST00000368474.8:c.3436G>T	ENSP00000357459.4:p.Val1146Leu
ENST00000492630.1:n.195G>T
ENST00000529168.1:c.3343G>T	ENSP00000431794.1:p.Val1115Leu
NM_001025107.2:c.2551G>T	NP_001020278.1:p.Val851Leu
NM_001111.4:c.3436G>T	NP_001102.2:p.Val1146Leu
NM_001193495.1:c.2551G>T	NP_001180424.1:p.Val851Leu
NM_015840.3:c.3358G>T	NP_056655.2:p.Val1120Leu
NM_015841.3:c.3301G>T	NP_056656.2:p.Val1101Leu
XM_006711109.1:c.3466G>T	XP_006711172.1:p.Val1156Leu
XM_006711111.2:c.2551G>T	XP_006711174.1:p.Val851Leu
XM_006711112.1:c.2551G>T	XP_006711175.1:p.Val851Leu
XM_006711113.1:c.2551G>T	XP_006711176.1:p.Val851Leu
XM_011509060.1:c.3565G>T	XP_011507362.1:p.Val1189Leu
XM_011509061.1:c.3487G>T	XP_011507363.1:p.Val1163Leu
XM_011509062.1:c.3454G>T	XP_011507364.1:p.Val1152Leu
NM_001025107.3:c.2551G>T	NP_001020278.1:p.Val851Leu
NM_001111.5:c.3436G>T MANE Select	NP_001102.3:p.Val1146Leu
NM_001193495.2:c.2551G>T	NP_001180424.1:p.Val851Leu
NM_001365045.1:c.3463G>T	NP_001351974.1:p.Val1155Leu
NM_001365046.1:c.2551G>T	NP_001351975.1:p.Val851Leu
NM_001365047.1:c.2551G>T	NP_001351976.1:p.Val851Leu
NM_001365048.1:c.2551G>T	NP_001351977.1:p.Val851Leu
NM_001365049.1:c.2473G>T	NP_001351978.1:p.Val825Leu
NM_015840.4:c.3358G>T	NP_056655.3:p.Val1120Leu
NM_015841.4:c.3301G>T	NP_056656.3:p.Val1101Leu
XM_006711113.2:c.2551G>T	XP_006711176.1:p.Val851Leu
XM_011509061.2:c.2473G>T	XP_011507363.2:p.Val825Leu
XM_024449674.1:c.3565G>T	XP_024305442.1:p.Val1189Leu