Canonical Allele Identifier: CA2648177888

Gene: ADAR

Linked Data

• gnomAD v4: 1-154588088-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588092del , CM000663.2:g.154588092del	GRCh38
NC_000001.10:g.154560568del , CM000663.1:g.154560568del	GRCh37
NC_000001.9:g.152827192del	NCBI36
NG_011844.1:g.44873del
NG_011844.2:g.48472del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2913+36del	ENSP00000497790.2:n.2913+36del
ENST00000649724.2:c.3049+36del	ENSP00000497932.2:n.3049+36del
ENST00000680270.2:c.2902+36del	ENSP00000505532.2:n.2902+36del
ENST00000681056.2:c.2671+36del	ENSP00000506234.2:n.2671+36del
ENST00000368471.8:c.2134+36del	ENSP00000357456.3:n.2134+36del
ENST00000368474.9:c.3019+36del MANE Select	ENSP00000357459.4:n.3019+36del
ENST00000529168.2:c.2941+36del	ENSP00000431794.2:n.2941+36del
ENST00000647682.2:n.3004+36del
ENST00000648231.2:c.2134+36del	ENSP00000497555.1:n.2134+36del
ENST00000648311.1:c.2134+36del	ENSP00000498137.1:n.2134+36del
ENST00000648714.2:c.*494+36del	ENSP00000497434.2:n.*494+36del
ENST00000649021.1:n.3347+36del
ENST00000649022.2:c.2134+36del	ENSP00000496896.2:n.2134+36del
ENST00000649042.1:c.2134+36del	ENSP00000497790.1:n.2134+36del
ENST00000649408.2:c.3019+36del	ENSP00000497386.2:n.3019+36del
ENST00000649724.1:c.2134+36del	ENSP00000497932.1:n.2134+36del
ENST00000649749.1:c.2134+36del	ENSP00000497210.1:n.2134+36del
ENST00000679375.1:c.*1251+36del	ENSP00000505887.1:n.*1251+36del
ENST00000679465.1:n.3472+36del
ENST00000679805.1:n.3347+36del
ENST00000679899.1:c.2077+36del	ENSP00000505996.1:n.2077+36del
ENST00000680270.1:c.2134+36del	ENSP00000505532.1:n.2134+36del
ENST00000680305.1:c.3019+36del	ENSP00000506312.1:n.3019+36del
ENST00000681056.1:c.2134+36del	ENSP00000506234.1:n.2134+36del
ENST00000681235.1:c.*2541+36del	ENSP00000506606.1:n.*2541+36del
ENST00000681429.1:n.2279+36del
ENST00000681683.1:c.2134+36del	ENSP00000506666.1:n.2134+36del
ENST00000681786.1:n.3472+36del
ENST00000681901.1:c.*2619+36del	ENSP00000504883.1:n.*2619+36del
ENST00000368471.7:c.2134+36del	ENSP00000357456.3:n.2134+36del
ENST00000368474.8:c.3019+36del	ENSP00000357459.4:n.3019+36del
ENST00000529168.1:c.2926+36del	ENSP00000431794.1:n.2926+36del
ENST00000530954.1:n.156+36del
ENST00000534279.1:n.478+36del
NM_001025107.2:c.2134+36del	NP_001020278.1:n.2134+36del
NM_001111.4:c.3019+36del	NP_001102.2:n.3019+36del
NM_001193495.1:c.2134+36del	NP_001180424.1:n.2134+36del
NM_015840.3:c.2941+36del	NP_056655.2:n.2941+36del
NM_015841.3:c.2884+36del	NP_056656.2:n.2884+36del
XM_006711109.1:c.3049+36del	XP_006711172.1:n.3049+36del
XM_006711111.2:c.2134+36del	XP_006711174.1:n.2134+36del
XM_006711112.1:c.2134+36del	XP_006711175.1:n.2134+36del
XM_006711113.1:c.2134+36del	XP_006711176.1:n.2134+36del
XM_011509060.1:c.3148+36del	XP_011507362.1:n.3148+36del
XM_011509061.1:c.3070+36del	XP_011507363.1:n.3070+36del
XM_011509062.1:c.3037+36del	XP_011507364.1:n.3037+36del
NM_001025107.3:c.2134+36del	NP_001020278.1:n.2134+36del
NM_001111.5:c.3019+36del MANE Select	NP_001102.3:n.3019+36del
NM_001193495.2:c.2134+36del	NP_001180424.1:n.2134+36del
NM_001365045.1:c.3046+36del	NP_001351974.1:n.3046+36del
NM_001365046.1:c.2134+36del	NP_001351975.1:n.2134+36del
NM_001365047.1:c.2134+36del	NP_001351976.1:n.2134+36del
NM_001365048.1:c.2134+36del	NP_001351977.1:n.2134+36del
NM_001365049.1:c.2056+36del	NP_001351978.1:n.2056+36del
NM_015840.4:c.2941+36del	NP_056655.3:n.2941+36del
NM_015841.4:c.2884+36del	NP_056656.3:n.2884+36del
XM_006711113.2:c.2134+36del	XP_006711176.1:n.2134+36del
XM_011509061.2:c.2056+36del	XP_011507363.2:n.2056+36del
XM_024449674.1:c.3148+36del	XP_024305442.1:n.3148+36del