Canonical Allele Identifier: CA2480938607
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154602320A= , CM000663.2:g.154602320A= GRCh38
NC_000001.10:g.154574796A= , CM000663.1:g.154574796A= GRCh37
NC_000001.9:g.152841420A= NCBI36
NG_011844.1:g.30642T=
NG_011844.2:g.34241T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.287+65T= ENSP00000497790.2:n.287+65T=
ENST00000649724.2:c.352T= ENSP00000497932.2:p.Phe118=
ENST00000680270.2:c.352T= ENSP00000505532.2:p.Phe118=
ENST00000681056.2:c.46-72T= ENSP00000506234.2:n.46-72T=
ENST00000368471.8:c.-564T= ENSP00000357456.3:n.-564T=
ENST00000368474.9:c.322T= MANE Select ENSP00000357459.4:p.Phe108=
ENST00000471068.2:n.390+65T=
ENST00000526905.2:n.257+65T=
ENST00000529168.2:c.322T= ENSP00000431794.2:p.Phe108=
ENST00000647682.2:n.124-72T=
ENST00000648231.2:c.-564T= ENSP00000497555.1:n.-564T=
ENST00000648311.1:c.-564T= ENSP00000498137.1:n.-564T=
ENST00000648714.2:c.322T= ENSP00000497434.2:p.Phe108=
ENST00000648871.1:c.-492-72T= ENSP00000497793.1:n.-492-72T=
ENST00000649021.1:n.358T=
ENST00000649022.2:c.-564T= ENSP00000496896.2:n.-564T=
ENST00000649042.1:c.-493+65T= ENSP00000497790.1:n.-493+65T=
ENST00000649408.2:c.322T= ENSP00000497386.2:p.Phe108=
ENST00000649724.1:c.-564T= ENSP00000497932.1:n.-564T=
ENST00000649749.1:c.-564T= ENSP00000497210.1:n.-564T=
ENST00000679375.1:c.-492-72T= ENSP00000505887.1:n.-492-72T=
ENST00000679465.1:n.520T=
ENST00000679805.1:n.358T=
ENST00000679899.1:c.-564T= ENSP00000505996.1:n.-564T=
ENST00000680270.1:c.-417T= ENSP00000505532.1:n.-417T=
ENST00000680305.1:c.322T= ENSP00000506312.1:p.Phe108=
ENST00000680472.1:n.361T=
ENST00000681056.1:c.-492-72T= ENSP00000506234.1:n.-492-72T=
ENST00000681235.1:c.257+65T= ENSP00000506606.1:n.257+65T=
ENST00000681683.1:c.-493+65T= ENSP00000506666.1:n.-493+65T=
ENST00000681786.1:n.520T=
ENST00000681901.1:c.257+65T= ENSP00000504883.1:n.257+65T=
ENST00000368471.7:c.-564T= ENSP00000357456.3:n.-564T=
ENST00000368474.8:c.322T= ENSP00000357459.4:p.Phe108=
ENST00000463920.5:n.275+65T=
ENST00000471068.1:n.353T=
ENST00000494866.1:n.300+65T=
ENST00000526905.1:n.369T=
ENST00000529168.1:c.307T= ENSP00000431794.1:p.Phe103=
NM_001025107.2:c.-564T= NP_001020278.1:n.-564T=
NM_001111.4:c.322T= NP_001102.2:p.Phe108=
NM_001193495.1:c.-564T= NP_001180424.1:n.-564T=
NM_015840.3:c.322T= NP_056655.2:p.Phe108=
NM_015841.3:c.322T= NP_056656.2:p.Phe108=
XM_006711109.1:c.352T= XP_006711172.1:p.Phe118=
XM_006711111.2:c.-493+65T= XP_006711174.1:n.-493+65T=
XM_006711112.1:c.-493+65T= XP_006711175.1:n.-493+65T=
XM_006711113.1:c.-493+65T= XP_006711176.1:n.-493+65T=
XM_011509060.1:c.451T= XP_011507362.1:p.Phe151=
XM_011509061.1:c.451T= XP_011507363.1:p.Phe151=
XM_011509062.1:c.340T= XP_011507364.1:p.Phe114=
NM_001025107.3:c.-564T= NP_001020278.1:n.-564T=
NM_001111.5:c.322T= MANE Select NP_001102.3:p.Phe108=
NM_001193495.2:c.-564T= NP_001180424.1:n.-564T=
NM_001365045.1:c.349T= NP_001351974.1:p.Phe117=
NM_001365046.1:c.-493+65T= NP_001351975.1:n.-493+65T=
NM_001365047.1:c.-493+65T= NP_001351976.1:n.-493+65T=
NM_001365048.1:c.-564T= NP_001351977.1:n.-564T=
NM_001365049.1:c.-493+65T= NP_001351978.1:n.-493+65T=
NM_015840.4:c.322T= NP_056655.3:p.Phe108=
NM_015841.4:c.322T= NP_056656.3:p.Phe108=
XM_006711113.2:c.-493+65T= XP_006711176.1:n.-493+65T=
XM_011509061.2:c.-564T= XP_011507363.2:n.-564T=
XM_024449674.1:c.451T= XP_024305442.1:p.Phe151=