Canonical Allele Identifier: CA2480944421
Gene: ADAR HGNC NCBI

Linked Data

dbSNP Id: rs1698600638

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154615234A>C , CM000663.2:g.154615234A>C GRCh38
NC_000001.10:g.154587710A>C , CM000663.1:g.154587710A>C GRCh37
NC_000001.9:g.152854334A>C NCBI36
NG_011844.1:g.17728T>G
NG_011844.2:g.21327T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000649042.2:c.46-12608T>G ENSP00000497790.2:n.46-12608T>G
ENST00000649724.2:c.46-12608T>G ENSP00000497932.2:n.46-12608T>G
ENST00000680270.2:c.46-12608T>G ENSP00000505532.2:n.46-12608T>G
ENST00000681056.2:c.45+12720T>G ENSP00000506234.2:n.45+12720T>G
ENST00000368471.8:c.-870-12608T>G ENSP00000357456.3:n.-870-12608T>G
ENST00000471068.2:n.148+12202T>G
ENST00000648311.1:c.-871+12202T>G ENSP00000498137.1:n.-871+12202T>G
ENST00000649021.1:n.52-12608T>G
ENST00000649022.2:c.-871+9829T>G ENSP00000496896.2:n.-871+9829T>G
ENST00000649042.1:c.-734-12608T>G ENSP00000497790.1:n.-734-12608T>G
ENST00000649724.1:c.-870-12608T>G ENSP00000497932.1:n.-870-12608T>G
ENST00000679375.1:c.-493+12621T>G ENSP00000505887.1:n.-493+12621T>G
ENST00000679805.1:n.52-12608T>G
ENST00000679899.1:c.-870-12608T>G ENSP00000505996.1:n.-870-12608T>G
ENST00000680270.1:c.-723-12608T>G ENSP00000505532.1:n.-723-12608T>G
ENST00000680472.1:n.55-12608T>G
ENST00000681056.1:c.-493+12720T>G ENSP00000506234.1:n.-493+12720T>G
ENST00000681683.1:c.-734-12608T>G ENSP00000506666.1:n.-734-12608T>G
ENST00000368471.7:c.-870-12608T>G ENSP00000357456.3:n.-870-12608T>G
ENST00000463920.5:n.34-12608T>G
ENST00000471068.1:n.47-12608T>G
ENST00000494866.1:n.59-12608T>G
NM_001025107.2:c.-870-12608T>G NP_001020278.1:n.-870-12608T>G
XM_006711109.1:c.46-12608T>G XP_006711172.1:n.46-12608T>G
XM_006711112.1:c.-734-12608T>G XP_006711175.1:n.-734-12608T>G
XM_006711113.1:c.-734-12608T>G XP_006711176.1:n.-734-12608T>G
XM_011509060.1:c.145-12608T>G XP_011507362.1:n.145-12608T>G
XM_011509061.1:c.145-12608T>G XP_011507363.1:n.145-12608T>G
XM_011509062.1:c.33+9829T>G XP_011507364.1:n.33+9829T>G
NM_001025107.3:c.-870-12608T>G NP_001020278.1:n.-870-12608T>G
NM_001365045.1:c.43-12608T>G NP_001351974.1:n.43-12608T>G
NM_001365046.1:c.-734-12608T>G NP_001351975.1:n.-734-12608T>G
XM_006711113.2:c.-734-12608T>G XP_006711176.1:n.-734-12608T>G
XM_011509061.2:c.-870-12608T>G XP_011507363.2:n.-870-12608T>G
XM_024449674.1:c.145-12608T>G XP_024305442.1:n.145-12608T>G