Canonical Allele Identifier: CA342636754

Gene: ADAR

Linked Data

• ClinVar Variation Id: 2944550
• ClinVar RCV Id: RCV003808252
• MyVariant Identifiers: chr1:g.154562239C>G (hg19) ; chr1:g.154589763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589763C>G , CM000663.2:g.154589763C>G	GRCh38
NC_000001.10:g.154562239C>G , CM000663.1:g.154562239C>G	GRCh37
NC_000001.9:g.152828863C>G	NCBI36
NG_011844.1:g.43199G>C
NG_011844.2:g.46798G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2556G>C	ENSP00000497790.2:n.2556G>C
ENST00000649724.2:c.2692G>C	ENSP00000497932.2:p.Gly898Arg
ENST00000680270.2:c.2545G>C	ENSP00000505532.2:p.Gly849Arg
ENST00000681056.2:c.2314G>C	ENSP00000506234.2:p.Gly772Arg
ENST00000368471.8:c.1777G>C	ENSP00000357456.3:p.Gly593Arg
ENST00000368474.9:c.2662G>C MANE Select	ENSP00000357459.4:p.Gly888Arg
ENST00000529168.2:c.2584G>C	ENSP00000431794.2:p.Gly862Arg
ENST00000647682.2:n.2647G>C
ENST00000648231.2:c.1777G>C	ENSP00000497555.1:p.Gly593Arg
ENST00000648311.1:c.1777G>C	ENSP00000498137.1:p.Gly593Arg
ENST00000648714.2:c.*137G>C	ENSP00000497434.2:n.*137G>C
ENST00000649021.1:n.2698G>C
ENST00000649022.2:c.1777G>C	ENSP00000496896.2:p.Gly593Arg
ENST00000649042.1:c.1777G>C	ENSP00000497790.1:p.Gly593Arg
ENST00000649408.2:c.2662G>C	ENSP00000497386.2:p.Gly888Arg
ENST00000649724.1:c.1777G>C	ENSP00000497932.1:p.Gly593Arg
ENST00000649749.1:c.1777G>C	ENSP00000497210.1:p.Gly593Arg
ENST00000679375.1:c.*894G>C	ENSP00000505887.1:n.*894G>C
ENST00000679465.1:n.3115G>C
ENST00000679805.1:n.2698G>C
ENST00000679899.1:c.1720G>C	ENSP00000505996.1:p.Gly574Arg
ENST00000680270.1:c.1777G>C	ENSP00000505532.1:p.Gly593Arg
ENST00000680305.1:c.2662G>C	ENSP00000506312.1:p.Gly888Arg
ENST00000681056.1:c.1777G>C	ENSP00000506234.1:p.Gly593Arg
ENST00000681235.1:c.*2184G>C	ENSP00000506606.1:n.*2184G>C
ENST00000681429.1:n.1922G>C
ENST00000681683.1:c.1777G>C	ENSP00000506666.1:p.Gly593Arg
ENST00000681786.1:n.3115G>C
ENST00000681901.1:c.*2262G>C	ENSP00000504883.1:n.*2262G>C
ENST00000368471.7:c.1777G>C	ENSP00000357456.3:p.Gly593Arg
ENST00000368474.8:c.2662G>C	ENSP00000357459.4:p.Gly888Arg
ENST00000529168.1:c.2569G>C	ENSP00000431794.1:p.Gly857Arg
NM_001025107.2:c.1777G>C	NP_001020278.1:p.Gly593Arg
NM_001111.4:c.2662G>C	NP_001102.2:p.Gly888Arg
NM_001193495.1:c.1777G>C	NP_001180424.1:p.Gly593Arg
NM_015840.3:c.2584G>C	NP_056655.2:p.Gly862Arg
NM_015841.3:c.2527G>C	NP_056656.2:p.Gly843Arg
XM_006711109.1:c.2692G>C	XP_006711172.1:p.Gly898Arg
XM_006711111.2:c.1777G>C	XP_006711174.1:p.Gly593Arg
XM_006711112.1:c.1777G>C	XP_006711175.1:p.Gly593Arg
XM_006711113.1:c.1777G>C	XP_006711176.1:p.Gly593Arg
XM_011509060.1:c.2791G>C	XP_011507362.1:p.Gly931Arg
XM_011509061.1:c.2713G>C	XP_011507363.1:p.Gly905Arg
XM_011509062.1:c.2680G>C	XP_011507364.1:p.Gly894Arg
NM_001025107.3:c.1777G>C	NP_001020278.1:p.Gly593Arg
NM_001111.5:c.2662G>C MANE Select	NP_001102.3:p.Gly888Arg
NM_001193495.2:c.1777G>C	NP_001180424.1:p.Gly593Arg
NM_001365045.1:c.2689G>C	NP_001351974.1:p.Gly897Arg
NM_001365046.1:c.1777G>C	NP_001351975.1:p.Gly593Arg
NM_001365047.1:c.1777G>C	NP_001351976.1:p.Gly593Arg
NM_001365048.1:c.1777G>C	NP_001351977.1:p.Gly593Arg
NM_001365049.1:c.1699G>C	NP_001351978.1:p.Gly567Arg
NM_015840.4:c.2584G>C	NP_056655.3:p.Gly862Arg
NM_015841.4:c.2527G>C	NP_056656.3:p.Gly843Arg
XM_006711113.2:c.1777G>C	XP_006711176.1:p.Gly593Arg
XM_011509061.2:c.1699G>C	XP_011507363.2:p.Gly567Arg
XM_024449674.1:c.2791G>C	XP_024305442.1:p.Gly931Arg