Canonical Allele Identifier: CA2480932543
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588226T= , CM000663.2:g.154588226T= GRCh38
NC_000001.10:g.154560702T= , CM000663.1:g.154560702T= GRCh37
NC_000001.9:g.152827326T= NCBI36
NG_011844.1:g.44736A=
NG_011844.2:g.48335A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2812A= ENSP00000497790.2:n.2812A=
ENST00000649724.2:c.2948A= ENSP00000497932.2:p.Asp983=
ENST00000680270.2:c.2801A= ENSP00000505532.2:p.Asp934=
ENST00000681056.2:c.2570A= ENSP00000506234.2:p.Asp857=
ENST00000368471.8:c.2033A= ENSP00000357456.3:p.Asp678=
ENST00000368474.9:c.2918A= MANE Select ENSP00000357459.4:p.Asp973=
ENST00000529168.2:c.2840A= ENSP00000431794.2:p.Asp947=
ENST00000647682.2:n.2903A=
ENST00000648231.2:c.2033A= ENSP00000497555.1:p.Asp678=
ENST00000648311.1:c.2033A= ENSP00000498137.1:p.Asp678=
ENST00000648714.2:c.*393A= ENSP00000497434.2:n.*393A=
ENST00000649021.1:n.3246A=
ENST00000649022.2:c.2033A= ENSP00000496896.2:p.Asp678=
ENST00000649042.1:c.2033A= ENSP00000497790.1:p.Asp678=
ENST00000649408.2:c.2918A= ENSP00000497386.2:p.Asp973=
ENST00000649724.1:c.2033A= ENSP00000497932.1:p.Asp678=
ENST00000649749.1:c.2033A= ENSP00000497210.1:p.Asp678=
ENST00000679375.1:c.*1150A= ENSP00000505887.1:n.*1150A=
ENST00000679465.1:n.3371A=
ENST00000679805.1:n.3246A=
ENST00000679899.1:c.1976A= ENSP00000505996.1:p.Asp659=
ENST00000680270.1:c.2033A= ENSP00000505532.1:p.Asp678=
ENST00000680305.1:c.2918A= ENSP00000506312.1:p.Asp973=
ENST00000681056.1:c.2033A= ENSP00000506234.1:p.Asp678=
ENST00000681235.1:c.*2440A= ENSP00000506606.1:n.*2440A=
ENST00000681429.1:n.2178A=
ENST00000681683.1:c.2033A= ENSP00000506666.1:p.Asp678=
ENST00000681786.1:n.3371A=
ENST00000681901.1:c.*2518A= ENSP00000504883.1:n.*2518A=
ENST00000368471.7:c.2033A= ENSP00000357456.3:p.Asp678=
ENST00000368474.8:c.2918A= ENSP00000357459.4:p.Asp973=
ENST00000529168.1:c.2825A= ENSP00000431794.1:p.Asp942=
ENST00000530954.1:n.55A=
ENST00000534279.1:n.377A=
NM_001025107.2:c.2033A= NP_001020278.1:p.Asp678=
NM_001111.4:c.2918A= NP_001102.2:p.Asp973=
NM_001193495.1:c.2033A= NP_001180424.1:p.Asp678=
NM_015840.3:c.2840A= NP_056655.2:p.Asp947=
NM_015841.3:c.2783A= NP_056656.2:p.Asp928=
XM_006711109.1:c.2948A= XP_006711172.1:p.Asp983=
XM_006711111.2:c.2033A= XP_006711174.1:p.Asp678=
XM_006711112.1:c.2033A= XP_006711175.1:p.Asp678=
XM_006711113.1:c.2033A= XP_006711176.1:p.Asp678=
XM_011509060.1:c.3047A= XP_011507362.1:p.Asp1016=
XM_011509061.1:c.2969A= XP_011507363.1:p.Asp990=
XM_011509062.1:c.2936A= XP_011507364.1:p.Asp979=
NM_001025107.3:c.2033A= NP_001020278.1:p.Asp678=
NM_001111.5:c.2918A= MANE Select NP_001102.3:p.Asp973=
NM_001193495.2:c.2033A= NP_001180424.1:p.Asp678=
NM_001365045.1:c.2945A= NP_001351974.1:p.Asp982=
NM_001365046.1:c.2033A= NP_001351975.1:p.Asp678=
NM_001365047.1:c.2033A= NP_001351976.1:p.Asp678=
NM_001365048.1:c.2033A= NP_001351977.1:p.Asp678=
NM_001365049.1:c.1955A= NP_001351978.1:p.Asp652=
NM_015840.4:c.2840A= NP_056655.3:p.Asp947=
NM_015841.4:c.2783A= NP_056656.3:p.Asp928=
XM_006711113.2:c.2033A= XP_006711176.1:p.Asp678=
XM_011509061.2:c.1955A= XP_011507363.2:p.Asp652=
XM_024449674.1:c.3047A= XP_024305442.1:p.Asp1016=