Canonical Allele Identifier: CA2480944429
Gene: ADAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154615246_154615247delinsGA , CM000663.2:g.154615246_154615247delinsGA GRCh38
NC_000001.10:g.154587722_154587723delinsGA , CM000663.1:g.154587722_154587723delinsGA GRCh37
NC_000001.9:g.152854346_152854347delinsGA NCBI36
NG_011844.1:g.17715_17716delinsTC
NG_011844.2:g.21314_21315delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000649042.2:c.46-12621_46-12620delinsTC ENSP00000497790.2:n.46-12621_46-12620delinsTC
ENST00000649724.2:c.46-12621_46-12620delinsTC ENSP00000497932.2:n.46-12621_46-12620delinsTC
ENST00000680270.2:c.46-12621_46-12620delinsTC ENSP00000505532.2:n.46-12621_46-12620delinsTC
ENST00000681056.2:c.45+12707_45+12708delinsTC ENSP00000506234.2:n.45+12707_45+12708delinsTC
ENST00000368471.8:c.-871+12608_-871+12609delinsTC ENSP00000357456.3:n.-871+12608_-871+12609delinsTC
ENST00000471068.2:n.148+12189_148+12190delinsTC
ENST00000648311.1:c.-871+12189_-871+12190delinsTC ENSP00000498137.1:n.-871+12189_-871+12190delinsTC
ENST00000649021.1:n.52-12621_52-12620delinsTC
ENST00000649022.2:c.-871+9816_-871+9817delinsTC ENSP00000496896.2:n.-871+9816_-871+9817delinsTC
ENST00000649042.1:c.-734-12621_-734-12620delinsTC ENSP00000497790.1:n.-734-12621_-734-12620delinsTC
ENST00000649724.1:c.-870-12621_-870-12620delinsTC ENSP00000497932.1:n.-870-12621_-870-12620delinsTC
ENST00000679375.1:c.-493+12608_-493+12609delinsTC ENSP00000505887.1:n.-493+12608_-493+12609delinsTC
ENST00000679805.1:n.52-12621_52-12620delinsTC
ENST00000679899.1:c.-871+12608_-871+12609delinsTC ENSP00000505996.1:n.-871+12608_-871+12609delinsTC
ENST00000680270.1:c.-723-12621_-723-12620delinsTC ENSP00000505532.1:n.-723-12621_-723-12620delinsTC
ENST00000680472.1:n.55-12621_55-12620delinsTC
ENST00000681056.1:c.-493+12707_-493+12708delinsTC ENSP00000506234.1:n.-493+12707_-493+12708delinsTC
ENST00000681683.1:c.-735+12608_-735+12609delinsTC ENSP00000506666.1:n.-735+12608_-735+12609delinsTC
ENST00000368471.7:c.-871+12608_-871+12609delinsTC ENSP00000357456.3:n.-871+12608_-871+12609delinsTC
ENST00000463920.5:n.34-12621_34-12620delinsTC
ENST00000471068.1:n.47-12621_47-12620delinsTC
ENST00000494866.1:n.58+12608_58+12609delinsTC
NM_001025107.2:c.-871+12608_-871+12609delinsTC NP_001020278.1:n.-871+12608_-871+12609delinsTC
XM_006711109.1:c.46-12621_46-12620delinsTC XP_006711172.1:n.46-12621_46-12620delinsTC
XM_006711112.1:c.-734-12621_-734-12620delinsTC XP_006711175.1:n.-734-12621_-734-12620delinsTC
XM_006711113.1:c.-735+12608_-735+12609delinsTC XP_006711176.1:n.-735+12608_-735+12609delinsTC
XM_011509060.1:c.144+12608_144+12609delinsTC XP_011507362.1:n.144+12608_144+12609delinsTC
XM_011509061.1:c.144+12608_144+12609delinsTC XP_011507363.1:n.144+12608_144+12609delinsTC
XM_011509062.1:c.33+9816_33+9817delinsTC XP_011507364.1:n.33+9816_33+9817delinsTC
NM_001025107.3:c.-871+12608_-871+12609delinsTC NP_001020278.1:n.-871+12608_-871+12609delinsTC
NM_001365045.1:c.43-12621_43-12620delinsTC NP_001351974.1:n.43-12621_43-12620delinsTC
NM_001365046.1:c.-734-12621_-734-12620delinsTC NP_001351975.1:n.-734-12621_-734-12620delinsTC
XM_006711113.2:c.-735+12608_-735+12609delinsTC XP_006711176.1:n.-735+12608_-735+12609delinsTC
XM_011509061.2:c.-871+12608_-871+12609delinsTC XP_011507363.2:n.-871+12608_-871+12609delinsTC
XM_024449674.1:c.144+12608_144+12609delinsTC XP_024305442.1:n.144+12608_144+12609delinsTC