Canonical Allele Identifier: CA2746190521

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154615242A>G , CM000663.2:g.154615242A>G	GRCh38
NC_000001.10:g.154587718A>G , CM000663.1:g.154587718A>G	GRCh37
NC_000001.9:g.152854342A>G	NCBI36
NG_011844.1:g.17720T>C
NG_011844.2:g.21319T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.46-12616T>C	ENSP00000497790.2:n.46-12616T>C
ENST00000649724.2:c.46-12616T>C	ENSP00000497932.2:n.46-12616T>C
ENST00000680270.2:c.46-12616T>C	ENSP00000505532.2:n.46-12616T>C
ENST00000681056.2:c.45+12712T>C	ENSP00000506234.2:n.45+12712T>C
ENST00000368471.8:c.-871+12613T>C	ENSP00000357456.3:n.-871+12613T>C
ENST00000471068.2:n.148+12194T>C
ENST00000648311.1:c.-871+12194T>C	ENSP00000498137.1:n.-871+12194T>C
ENST00000649021.1:n.52-12616T>C
ENST00000649022.2:c.-871+9821T>C	ENSP00000496896.2:n.-871+9821T>C
ENST00000649042.1:c.-734-12616T>C	ENSP00000497790.1:n.-734-12616T>C
ENST00000649724.1:c.-870-12616T>C	ENSP00000497932.1:n.-870-12616T>C
ENST00000679375.1:c.-493+12613T>C	ENSP00000505887.1:n.-493+12613T>C
ENST00000679805.1:n.52-12616T>C
ENST00000679899.1:c.-871+12613T>C	ENSP00000505996.1:n.-871+12613T>C
ENST00000680270.1:c.-723-12616T>C	ENSP00000505532.1:n.-723-12616T>C
ENST00000680472.1:n.55-12616T>C
ENST00000681056.1:c.-493+12712T>C	ENSP00000506234.1:n.-493+12712T>C
ENST00000681683.1:c.-735+12613T>C	ENSP00000506666.1:n.-735+12613T>C
ENST00000368471.7:c.-871+12613T>C	ENSP00000357456.3:n.-871+12613T>C
ENST00000463920.5:n.34-12616T>C
ENST00000471068.1:n.47-12616T>C
ENST00000494866.1:n.58+12613T>C
NM_001025107.2:c.-871+12613T>C	NP_001020278.1:n.-871+12613T>C
XM_006711109.1:c.46-12616T>C	XP_006711172.1:n.46-12616T>C
XM_006711112.1:c.-734-12616T>C	XP_006711175.1:n.-734-12616T>C
XM_006711113.1:c.-735+12613T>C	XP_006711176.1:n.-735+12613T>C
XM_011509060.1:c.144+12613T>C	XP_011507362.1:n.144+12613T>C
XM_011509061.1:c.144+12613T>C	XP_011507363.1:n.144+12613T>C
XM_011509062.1:c.33+9821T>C	XP_011507364.1:n.33+9821T>C
NM_001025107.3:c.-871+12613T>C	NP_001020278.1:n.-871+12613T>C
NM_001365045.1:c.43-12616T>C	NP_001351974.1:n.43-12616T>C
NM_001365046.1:c.-734-12616T>C	NP_001351975.1:n.-734-12616T>C
XM_006711113.2:c.-735+12613T>C	XP_006711176.1:n.-735+12613T>C
XM_011509061.2:c.-871+12613T>C	XP_011507363.2:n.-871+12613T>C
XM_024449674.1:c.144+12613T>C	XP_024305442.1:n.144+12613T>C