Canonical Allele Identifier: CA2480932523
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154588188A= , CM000663.2:g.154588188A= GRCh38
NC_000001.10:g.154560664A= , CM000663.1:g.154560664A= GRCh37
NC_000001.9:g.152827288A= NCBI36
NG_011844.1:g.44774T=
NG_011844.2:g.48373T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.2850T= ENSP00000497790.2:n.2850T=
ENST00000649724.2:c.2986T= ENSP00000497932.2:p.Ser996=
ENST00000680270.2:c.2839T= ENSP00000505532.2:p.Ser947=
ENST00000681056.2:c.2608T= ENSP00000506234.2:p.Ser870=
ENST00000368471.8:c.2071T= ENSP00000357456.3:p.Ser691=
ENST00000368474.9:c.2956T= MANE Select ENSP00000357459.4:p.Ser986=
ENST00000529168.2:c.2878T= ENSP00000431794.2:p.Ser960=
ENST00000647682.2:n.2941T=
ENST00000648231.2:c.2071T= ENSP00000497555.1:p.Ser691=
ENST00000648311.1:c.2071T= ENSP00000498137.1:p.Ser691=
ENST00000648714.2:c.*431T= ENSP00000497434.2:n.*431T=
ENST00000649021.1:n.3284T=
ENST00000649022.2:c.2071T= ENSP00000496896.2:p.Ser691=
ENST00000649042.1:c.2071T= ENSP00000497790.1:p.Ser691=
ENST00000649408.2:c.2956T= ENSP00000497386.2:p.Ser986=
ENST00000649724.1:c.2071T= ENSP00000497932.1:p.Ser691=
ENST00000649749.1:c.2071T= ENSP00000497210.1:p.Ser691=
ENST00000679375.1:c.*1188T= ENSP00000505887.1:n.*1188T=
ENST00000679465.1:n.3409T=
ENST00000679805.1:n.3284T=
ENST00000679899.1:c.2014T= ENSP00000505996.1:p.Ser672=
ENST00000680270.1:c.2071T= ENSP00000505532.1:p.Ser691=
ENST00000680305.1:c.2956T= ENSP00000506312.1:p.Ser986=
ENST00000681056.1:c.2071T= ENSP00000506234.1:p.Ser691=
ENST00000681235.1:c.*2478T= ENSP00000506606.1:n.*2478T=
ENST00000681429.1:n.2216T=
ENST00000681683.1:c.2071T= ENSP00000506666.1:p.Ser691=
ENST00000681786.1:n.3409T=
ENST00000681901.1:c.*2556T= ENSP00000504883.1:n.*2556T=
ENST00000368471.7:c.2071T= ENSP00000357456.3:p.Ser691=
ENST00000368474.8:c.2956T= ENSP00000357459.4:p.Ser986=
ENST00000529168.1:c.2863T= ENSP00000431794.1:p.Ser955=
ENST00000530954.1:n.93T=
ENST00000534279.1:n.415T=
NM_001025107.2:c.2071T= NP_001020278.1:p.Ser691=
NM_001111.4:c.2956T= NP_001102.2:p.Ser986=
NM_001193495.1:c.2071T= NP_001180424.1:p.Ser691=
NM_015840.3:c.2878T= NP_056655.2:p.Ser960=
NM_015841.3:c.2821T= NP_056656.2:p.Ser941=
XM_006711109.1:c.2986T= XP_006711172.1:p.Ser996=
XM_006711111.2:c.2071T= XP_006711174.1:p.Ser691=
XM_006711112.1:c.2071T= XP_006711175.1:p.Ser691=
XM_006711113.1:c.2071T= XP_006711176.1:p.Ser691=
XM_011509060.1:c.3085T= XP_011507362.1:p.Ser1029=
XM_011509061.1:c.3007T= XP_011507363.1:p.Ser1003=
XM_011509062.1:c.2974T= XP_011507364.1:p.Ser992=
NM_001025107.3:c.2071T= NP_001020278.1:p.Ser691=
NM_001111.5:c.2956T= MANE Select NP_001102.3:p.Ser986=
NM_001193495.2:c.2071T= NP_001180424.1:p.Ser691=
NM_001365045.1:c.2983T= NP_001351974.1:p.Ser995=
NM_001365046.1:c.2071T= NP_001351975.1:p.Ser691=
NM_001365047.1:c.2071T= NP_001351976.1:p.Ser691=
NM_001365048.1:c.2071T= NP_001351977.1:p.Ser691=
NM_001365049.1:c.1993T= NP_001351978.1:p.Ser665=
NM_015840.4:c.2878T= NP_056655.3:p.Ser960=
NM_015841.4:c.2821T= NP_056656.3:p.Ser941=
XM_006711113.2:c.2071T= XP_006711176.1:p.Ser691=
XM_011509061.2:c.1993T= XP_011507363.2:p.Ser665=
XM_024449674.1:c.3085T= XP_024305442.1:p.Ser1029=