Canonical Allele Identifier: CA2480932505
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588128T= , CM000663.2:g.154588128T= GRCh38
NC_000001.10:g.154560604T= , CM000663.1:g.154560604T= GRCh37
NC_000001.9:g.152827228T= NCBI36
NG_011844.1:g.44834A=
NG_011844.2:g.48433A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2910A= ENSP00000497790.2:n.2910A=
ENST00000649724.2:c.3046A= ENSP00000497932.2:p.Asn1016=
ENST00000680270.2:c.2899A= ENSP00000505532.2:p.Asn967=
ENST00000681056.2:c.2668A= ENSP00000506234.2:p.Asn890=
ENST00000368471.8:c.2131A= ENSP00000357456.3:p.Asn711=
ENST00000368474.9:c.3016A= MANE Select ENSP00000357459.4:p.Asn1006=
ENST00000529168.2:c.2938A= ENSP00000431794.2:p.Asn980=
ENST00000647682.2:n.3001A=
ENST00000648231.2:c.2131A= ENSP00000497555.1:p.Asn711=
ENST00000648311.1:c.2131A= ENSP00000498137.1:p.Asn711=
ENST00000648714.2:c.*491A= ENSP00000497434.2:n.*491A=
ENST00000649021.1:n.3344A=
ENST00000649022.2:c.2131A= ENSP00000496896.2:p.Asn711=
ENST00000649042.1:c.2131A= ENSP00000497790.1:p.Asn711=
ENST00000649408.2:c.3016A= ENSP00000497386.2:p.Asn1006=
ENST00000649724.1:c.2131A= ENSP00000497932.1:p.Asn711=
ENST00000649749.1:c.2131A= ENSP00000497210.1:p.Asn711=
ENST00000679375.1:c.*1248A= ENSP00000505887.1:n.*1248A=
ENST00000679465.1:n.3469A=
ENST00000679805.1:n.3344A=
ENST00000679899.1:c.2074A= ENSP00000505996.1:p.Asn692=
ENST00000680270.1:c.2131A= ENSP00000505532.1:p.Asn711=
ENST00000680305.1:c.3016A= ENSP00000506312.1:p.Asn1006=
ENST00000681056.1:c.2131A= ENSP00000506234.1:p.Asn711=
ENST00000681235.1:c.*2538A= ENSP00000506606.1:n.*2538A=
ENST00000681429.1:n.2276A=
ENST00000681683.1:c.2131A= ENSP00000506666.1:p.Asn711=
ENST00000681786.1:n.3469A=
ENST00000681901.1:c.*2616A= ENSP00000504883.1:n.*2616A=
ENST00000368471.7:c.2131A= ENSP00000357456.3:p.Asn711=
ENST00000368474.8:c.3016A= ENSP00000357459.4:p.Asn1006=
ENST00000529168.1:c.2923A= ENSP00000431794.1:p.Asn975=
ENST00000530954.1:n.153A=
ENST00000534279.1:n.475A=
NM_001025107.2:c.2131A= NP_001020278.1:p.Asn711=
NM_001111.4:c.3016A= NP_001102.2:p.Asn1006=
NM_001193495.1:c.2131A= NP_001180424.1:p.Asn711=
NM_015840.3:c.2938A= NP_056655.2:p.Asn980=
NM_015841.3:c.2881A= NP_056656.2:p.Asn961=
XM_006711109.1:c.3046A= XP_006711172.1:p.Asn1016=
XM_006711111.2:c.2131A= XP_006711174.1:p.Asn711=
XM_006711112.1:c.2131A= XP_006711175.1:p.Asn711=
XM_006711113.1:c.2131A= XP_006711176.1:p.Asn711=
XM_011509060.1:c.3145A= XP_011507362.1:p.Asn1049=
XM_011509061.1:c.3067A= XP_011507363.1:p.Asn1023=
XM_011509062.1:c.3034A= XP_011507364.1:p.Asn1012=
NM_001025107.3:c.2131A= NP_001020278.1:p.Asn711=
NM_001111.5:c.3016A= MANE Select NP_001102.3:p.Asn1006=
NM_001193495.2:c.2131A= NP_001180424.1:p.Asn711=
NM_001365045.1:c.3043A= NP_001351974.1:p.Asn1015=
NM_001365046.1:c.2131A= NP_001351975.1:p.Asn711=
NM_001365047.1:c.2131A= NP_001351976.1:p.Asn711=
NM_001365048.1:c.2131A= NP_001351977.1:p.Asn711=
NM_001365049.1:c.2053A= NP_001351978.1:p.Asn685=
NM_015840.4:c.2938A= NP_056655.3:p.Asn980=
NM_015841.4:c.2881A= NP_056656.3:p.Asn961=
XM_006711113.2:c.2131A= XP_006711176.1:p.Asn711=
XM_011509061.2:c.2053A= XP_011507363.2:p.Asn685=
XM_024449674.1:c.3145A= XP_024305442.1:p.Asn1049=