Canonical Allele Identifier: CA342635511

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154586180C>T , CM000663.2:g.154586180C>T	GRCh38
NC_000001.10:g.154558656C>T , CM000663.1:g.154558656C>T	GRCh37
NC_000001.9:g.152825280C>T	NCBI36
NG_011844.1:g.46782G>A
NG_011844.2:g.50381G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001111.5:c.3202+1G>A MANE Select	NP_001102.3:n.3202+1G>A
ENST00000368474.9:c.3202+1G>A MANE Select	ENSP00000357459.4:n.3202+1G>A
NM_001025107.2:c.2317+1G>A	NP_001020278.1:n.2317+1G>A
NM_001025107.3:c.2317+1G>A	NP_001020278.1:n.2317+1G>A
NM_001111.4:c.3202+1G>A	NP_001102.2:n.3202+1G>A
NM_001193495.1:c.2317+1G>A	NP_001180424.1:n.2317+1G>A
NM_001193495.2:c.2317+1G>A	NP_001180424.1:n.2317+1G>A
NM_001365045.1:c.3229+1G>A	NP_001351974.1:n.3229+1G>A
NM_001365046.1:c.2317+1G>A	NP_001351975.1:n.2317+1G>A
NM_001365047.1:c.2317+1G>A	NP_001351976.1:n.2317+1G>A
NM_001365048.1:c.2317+1G>A	NP_001351977.1:n.2317+1G>A
NM_001365049.1:c.2239+1G>A	NP_001351978.1:n.2239+1G>A
NM_015840.3:c.3124+1G>A	NP_056655.2:n.3124+1G>A
NM_015840.4:c.3124+1G>A	NP_056655.3:n.3124+1G>A
NM_015841.3:c.3067+1G>A	NP_056656.2:n.3067+1G>A
NM_015841.4:c.3067+1G>A	NP_056656.3:n.3067+1G>A
ENST00000368471.7:c.2317+1G>A	ENSP00000357456.3:n.2317+1G>A
ENST00000368471.8:c.2317+1G>A	ENSP00000357456.3:n.2317+1G>A
ENST00000368474.8:c.3202+1G>A	ENSP00000357459.4:n.3202+1G>A
ENST00000492630.2:n.1587+1G>A
ENST00000529168.1:c.3109+1G>A	ENSP00000431794.1:n.3109+1G>A
ENST00000529168.2:c.3124+1G>A	ENSP00000431794.2:n.3124+1G>A
ENST00000530954.1:n.339+1G>A
ENST00000534279.1:n.662G>A
ENST00000647682.2:n.3187+1G>A
ENST00000648231.2:c.2317+1G>A	ENSP00000497555.1:n.2317+1G>A
ENST00000648311.1:c.2317+1G>A	ENSP00000498137.1:n.2317+1G>A
ENST00000648714.2:c.*677+1G>A	ENSP00000497434.2:n.*677+1G>A
ENST00000649021.1:n.3530+1G>A
ENST00000649022.2:c.2317+1G>A	ENSP00000496896.2:n.2317+1G>A
ENST00000649042.1:c.2317+1G>A	ENSP00000497790.1:n.2317+1G>A
ENST00000649042.2:c.3096+1G>A	ENSP00000497790.2:n.3096+1G>A
ENST00000649408.2:c.*368+1G>A	ENSP00000497386.2:n.*368+1G>A
ENST00000649724.1:c.2317+1G>A	ENSP00000497932.1:n.2317+1G>A
ENST00000649724.2:c.3232+1G>A	ENSP00000497932.2:n.3232+1G>A
ENST00000649749.1:c.2317+1G>A	ENSP00000497210.1:n.2317+1G>A
ENST00000679375.1:c.*1434+1G>A	ENSP00000505887.1:n.*1434+1G>A
ENST00000679465.1:n.3655+1G>A
ENST00000679805.1:n.3530+1G>A
ENST00000679899.1:c.2260+1G>A	ENSP00000505996.1:n.2260+1G>A
ENST00000680270.1:c.2317+1G>A	ENSP00000505532.1:n.2317+1G>A
ENST00000680270.2:c.3085+1G>A	ENSP00000505532.2:n.3085+1G>A
ENST00000680305.1:c.3020-315G>A	ENSP00000506312.1:n.3020-315G>A
ENST00000681056.1:c.2317+1G>A	ENSP00000506234.1:n.2317+1G>A
ENST00000681056.2:c.2854+1G>A	ENSP00000506234.2:n.2854+1G>A
ENST00000681235.1:c.*2724+1G>A	ENSP00000506606.1:n.*2724+1G>A
ENST00000681429.1:n.2462+1G>A
ENST00000681683.1:c.2317+1G>A	ENSP00000506666.1:n.2317+1G>A
ENST00000681786.1:n.3655+1G>A
ENST00000681901.1:c.*2802+1G>A	ENSP00000504883.1:n.*2802+1G>A
XM_006711109.1:c.3232+1G>A	XP_006711172.1:n.3232+1G>A
XM_006711111.2:c.2317+1G>A	XP_006711174.1:n.2317+1G>A
XM_006711112.1:c.2317+1G>A	XP_006711175.1:n.2317+1G>A
XM_006711113.1:c.2317+1G>A	XP_006711176.1:n.2317+1G>A
XM_006711113.2:c.2317+1G>A	XP_006711176.1:n.2317+1G>A
XM_011509060.1:c.3331+1G>A	XP_011507362.1:n.3331+1G>A
XM_011509061.1:c.3253+1G>A	XP_011507363.1:n.3253+1G>A
XM_011509061.2:c.2239+1G>A	XP_011507363.2:n.2239+1G>A
XM_011509062.1:c.3220+1G>A	XP_011507364.1:n.3220+1G>A
XM_024449674.1:c.3331+1G>A	XP_024305442.1:n.3331+1G>A