Canonical Allele Identifier: CA342636050

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154560660C>G (hg19) ; chr1:g.154588184C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588184C>G , CM000663.2:g.154588184C>G	GRCh38
NC_000001.10:g.154560660C>G , CM000663.1:g.154560660C>G	GRCh37
NC_000001.9:g.152827284C>G	NCBI36
NG_011844.1:g.44778G>C
NG_011844.2:g.48377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2854G>C	ENSP00000497790.2:n.2854G>C
ENST00000649724.2:c.2990G>C	ENSP00000497932.2:p.Arg997Pro
ENST00000680270.2:c.2843G>C	ENSP00000505532.2:p.Arg948Pro
ENST00000681056.2:c.2612G>C	ENSP00000506234.2:p.Arg871Pro
ENST00000368471.8:c.2075G>C	ENSP00000357456.3:p.Arg692Pro
ENST00000368474.9:c.2960G>C MANE Select	ENSP00000357459.4:p.Arg987Pro
ENST00000529168.2:c.2882G>C	ENSP00000431794.2:p.Arg961Pro
ENST00000647682.2:n.2945G>C
ENST00000648231.2:c.2075G>C	ENSP00000497555.1:p.Arg692Pro
ENST00000648311.1:c.2075G>C	ENSP00000498137.1:p.Arg692Pro
ENST00000648714.2:c.*435G>C	ENSP00000497434.2:n.*435G>C
ENST00000649021.1:n.3288G>C
ENST00000649022.2:c.2075G>C	ENSP00000496896.2:p.Arg692Pro
ENST00000649042.1:c.2075G>C	ENSP00000497790.1:p.Arg692Pro
ENST00000649408.2:c.2960G>C	ENSP00000497386.2:p.Arg987Pro
ENST00000649724.1:c.2075G>C	ENSP00000497932.1:p.Arg692Pro
ENST00000649749.1:c.2075G>C	ENSP00000497210.1:p.Arg692Pro
ENST00000679375.1:c.*1192G>C	ENSP00000505887.1:n.*1192G>C
ENST00000679465.1:n.3413G>C
ENST00000679805.1:n.3288G>C
ENST00000679899.1:c.2018G>C	ENSP00000505996.1:p.Arg673Pro
ENST00000680270.1:c.2075G>C	ENSP00000505532.1:p.Arg692Pro
ENST00000680305.1:c.2960G>C	ENSP00000506312.1:p.Arg987Pro
ENST00000681056.1:c.2075G>C	ENSP00000506234.1:p.Arg692Pro
ENST00000681235.1:c.*2482G>C	ENSP00000506606.1:n.*2482G>C
ENST00000681429.1:n.2220G>C
ENST00000681683.1:c.2075G>C	ENSP00000506666.1:p.Arg692Pro
ENST00000681786.1:n.3413G>C
ENST00000681901.1:c.*2560G>C	ENSP00000504883.1:n.*2560G>C
ENST00000368471.7:c.2075G>C	ENSP00000357456.3:p.Arg692Pro
ENST00000368474.8:c.2960G>C	ENSP00000357459.4:p.Arg987Pro
ENST00000529168.1:c.2867G>C	ENSP00000431794.1:p.Arg956Pro
ENST00000530954.1:n.97G>C
ENST00000534279.1:n.419G>C
NM_001025107.2:c.2075G>C	NP_001020278.1:p.Arg692Pro
NM_001111.4:c.2960G>C	NP_001102.2:p.Arg987Pro
NM_001193495.1:c.2075G>C	NP_001180424.1:p.Arg692Pro
NM_015840.3:c.2882G>C	NP_056655.2:p.Arg961Pro
NM_015841.3:c.2825G>C	NP_056656.2:p.Arg942Pro
XM_006711109.1:c.2990G>C	XP_006711172.1:p.Arg997Pro
XM_006711111.2:c.2075G>C	XP_006711174.1:p.Arg692Pro
XM_006711112.1:c.2075G>C	XP_006711175.1:p.Arg692Pro
XM_006711113.1:c.2075G>C	XP_006711176.1:p.Arg692Pro
XM_011509060.1:c.3089G>C	XP_011507362.1:p.Arg1030Pro
XM_011509061.1:c.3011G>C	XP_011507363.1:p.Arg1004Pro
XM_011509062.1:c.2978G>C	XP_011507364.1:p.Arg993Pro
NM_001025107.3:c.2075G>C	NP_001020278.1:p.Arg692Pro
NM_001111.5:c.2960G>C MANE Select	NP_001102.3:p.Arg987Pro
NM_001193495.2:c.2075G>C	NP_001180424.1:p.Arg692Pro
NM_001365045.1:c.2987G>C	NP_001351974.1:p.Arg996Pro
NM_001365046.1:c.2075G>C	NP_001351975.1:p.Arg692Pro
NM_001365047.1:c.2075G>C	NP_001351976.1:p.Arg692Pro
NM_001365048.1:c.2075G>C	NP_001351977.1:p.Arg692Pro
NM_001365049.1:c.1997G>C	NP_001351978.1:p.Arg666Pro
NM_015840.4:c.2882G>C	NP_056655.3:p.Arg961Pro
NM_015841.4:c.2825G>C	NP_056656.3:p.Arg942Pro
XM_006711113.2:c.2075G>C	XP_006711176.1:p.Arg692Pro
XM_011509061.2:c.1997G>C	XP_011507363.2:p.Arg666Pro
XM_024449674.1:c.3089G>C	XP_024305442.1:p.Arg1030Pro