Canonical Allele Identifier: CA342636744

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589759-G-C
• MyVariant Identifiers: chr1:g.154562235G>C (hg19) ; chr1:g.154589759G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589759G>C , CM000663.2:g.154589759G>C	GRCh38
NC_000001.10:g.154562235G>C , CM000663.1:g.154562235G>C	GRCh37
NC_000001.9:g.152828859G>C	NCBI36
NG_011844.1:g.43203C>G
NG_011844.2:g.46802C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2560C>G	ENSP00000497790.2:n.2560C>G
ENST00000649724.2:c.2696C>G	ENSP00000497932.2:p.Thr899Arg
ENST00000680270.2:c.2549C>G	ENSP00000505532.2:p.Thr850Arg
ENST00000681056.2:c.2318C>G	ENSP00000506234.2:p.Thr773Arg
ENST00000368471.8:c.1781C>G	ENSP00000357456.3:p.Thr594Arg
ENST00000368474.9:c.2666C>G MANE Select	ENSP00000357459.4:p.Thr889Arg
ENST00000529168.2:c.2588C>G	ENSP00000431794.2:p.Thr863Arg
ENST00000647682.2:n.2651C>G
ENST00000648231.2:c.1781C>G	ENSP00000497555.1:p.Thr594Arg
ENST00000648311.1:c.1781C>G	ENSP00000498137.1:p.Thr594Arg
ENST00000648714.2:c.*141C>G	ENSP00000497434.2:n.*141C>G
ENST00000649021.1:n.2702C>G
ENST00000649022.2:c.1781C>G	ENSP00000496896.2:p.Thr594Arg
ENST00000649042.1:c.1781C>G	ENSP00000497790.1:p.Thr594Arg
ENST00000649408.2:c.2666C>G	ENSP00000497386.2:p.Thr889Arg
ENST00000649724.1:c.1781C>G	ENSP00000497932.1:p.Thr594Arg
ENST00000649749.1:c.1781C>G	ENSP00000497210.1:p.Thr594Arg
ENST00000679375.1:c.*898C>G	ENSP00000505887.1:n.*898C>G
ENST00000679465.1:n.3119C>G
ENST00000679805.1:n.2702C>G
ENST00000679899.1:c.1724C>G	ENSP00000505996.1:p.Thr575Arg
ENST00000680270.1:c.1781C>G	ENSP00000505532.1:p.Thr594Arg
ENST00000680305.1:c.2666C>G	ENSP00000506312.1:p.Thr889Arg
ENST00000681056.1:c.1781C>G	ENSP00000506234.1:p.Thr594Arg
ENST00000681235.1:c.*2188C>G	ENSP00000506606.1:n.*2188C>G
ENST00000681429.1:n.1926C>G
ENST00000681683.1:c.1781C>G	ENSP00000506666.1:p.Thr594Arg
ENST00000681786.1:n.3119C>G
ENST00000681901.1:c.*2266C>G	ENSP00000504883.1:n.*2266C>G
ENST00000368471.7:c.1781C>G	ENSP00000357456.3:p.Thr594Arg
ENST00000368474.8:c.2666C>G	ENSP00000357459.4:p.Thr889Arg
ENST00000529168.1:c.2573C>G	ENSP00000431794.1:p.Thr858Arg
NM_001025107.2:c.1781C>G	NP_001020278.1:p.Thr594Arg
NM_001111.4:c.2666C>G	NP_001102.2:p.Thr889Arg
NM_001193495.1:c.1781C>G	NP_001180424.1:p.Thr594Arg
NM_015840.3:c.2588C>G	NP_056655.2:p.Thr863Arg
NM_015841.3:c.2531C>G	NP_056656.2:p.Thr844Arg
XM_006711109.1:c.2696C>G	XP_006711172.1:p.Thr899Arg
XM_006711111.2:c.1781C>G	XP_006711174.1:p.Thr594Arg
XM_006711112.1:c.1781C>G	XP_006711175.1:p.Thr594Arg
XM_006711113.1:c.1781C>G	XP_006711176.1:p.Thr594Arg
XM_011509060.1:c.2795C>G	XP_011507362.1:p.Thr932Arg
XM_011509061.1:c.2717C>G	XP_011507363.1:p.Thr906Arg
XM_011509062.1:c.2684C>G	XP_011507364.1:p.Thr895Arg
NM_001025107.3:c.1781C>G	NP_001020278.1:p.Thr594Arg
NM_001111.5:c.2666C>G MANE Select	NP_001102.3:p.Thr889Arg
NM_001193495.2:c.1781C>G	NP_001180424.1:p.Thr594Arg
NM_001365045.1:c.2693C>G	NP_001351974.1:p.Thr898Arg
NM_001365046.1:c.1781C>G	NP_001351975.1:p.Thr594Arg
NM_001365047.1:c.1781C>G	NP_001351976.1:p.Thr594Arg
NM_001365048.1:c.1781C>G	NP_001351977.1:p.Thr594Arg
NM_001365049.1:c.1703C>G	NP_001351978.1:p.Thr568Arg
NM_015840.4:c.2588C>G	NP_056655.3:p.Thr863Arg
NM_015841.4:c.2531C>G	NP_056656.3:p.Thr844Arg
XM_006711113.2:c.1781C>G	XP_006711176.1:p.Thr594Arg
XM_011509061.2:c.1703C>G	XP_011507363.2:p.Thr568Arg
XM_024449674.1:c.2795C>G	XP_024305442.1:p.Thr932Arg