Canonical Allele Identifier: CA2746189695

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589799_154589800insA , CM000663.2:g.154589799_154589800insA	GRCh38
NC_000001.10:g.154562275_154562276insA , CM000663.1:g.154562275_154562276insA	GRCh37
NC_000001.9:g.152828899_152828900insA	NCBI36
NG_011844.1:g.43162_43163insT
NG_011844.2:g.46761_46762insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2519_2520insT	ENSP00000497790.2:n.2519_2520insT
ENST00000649724.2:c.2655_2656insT	ENSP00000497932.2:p.Lys886Ter
ENST00000680270.2:c.2508_2509insT	ENSP00000505532.2:p.Lys837Ter
ENST00000681056.2:c.2277_2278insT	ENSP00000506234.2:p.Lys760Ter
ENST00000368471.8:c.1740_1741insT	ENSP00000357456.3:p.Lys581Ter
ENST00000368474.9:c.2625_2626insT MANE Select	ENSP00000357459.4:p.Lys876Ter
ENST00000529168.2:c.2547_2548insT	ENSP00000431794.2:p.Lys850Ter
ENST00000647682.2:n.2610_2611insT
ENST00000648231.2:c.1740_1741insT	ENSP00000497555.1:p.Lys581Ter
ENST00000648311.1:c.1740_1741insT	ENSP00000498137.1:p.Lys581Ter
ENST00000648714.2:c.*100_*101insT	ENSP00000497434.2:n.*100_*101insT
ENST00000649021.1:n.2661_2662insT
ENST00000649022.2:c.1740_1741insT	ENSP00000496896.2:p.Lys581Ter
ENST00000649042.1:c.1740_1741insT	ENSP00000497790.1:p.Lys581Ter
ENST00000649408.2:c.2625_2626insT	ENSP00000497386.2:p.Lys876Ter
ENST00000649724.1:c.1740_1741insT	ENSP00000497932.1:p.Lys581Ter
ENST00000649749.1:c.1740_1741insT	ENSP00000497210.1:p.Lys581Ter
ENST00000679375.1:c.*857_*858insT	ENSP00000505887.1:n.*857_*858insT
ENST00000679465.1:n.3078_3079insT
ENST00000679805.1:n.2661_2662insT
ENST00000679899.1:c.1683_1684insT	ENSP00000505996.1:p.Lys562Ter
ENST00000680270.1:c.1740_1741insT	ENSP00000505532.1:p.Lys581Ter
ENST00000680305.1:c.2625_2626insT	ENSP00000506312.1:p.Lys876Ter
ENST00000681056.1:c.1740_1741insT	ENSP00000506234.1:p.Lys581Ter
ENST00000681235.1:c.*2147_*2148insT	ENSP00000506606.1:n.*2147_*2148insT
ENST00000681429.1:n.1885_1886insT
ENST00000681683.1:c.1740_1741insT	ENSP00000506666.1:p.Lys581Ter
ENST00000681786.1:n.3078_3079insT
ENST00000681901.1:c.*2225_*2226insT	ENSP00000504883.1:n.*2225_*2226insT
ENST00000368471.7:c.1740_1741insT	ENSP00000357456.3:p.Lys581Ter
ENST00000368474.8:c.2625_2626insT	ENSP00000357459.4:p.Lys876Ter
ENST00000529168.1:c.2532_2533insT	ENSP00000431794.1:p.Lys845Ter
NM_001025107.2:c.1740_1741insT	NP_001020278.1:p.Lys581Ter
NM_001111.4:c.2625_2626insT	NP_001102.2:p.Lys876Ter
NM_001193495.1:c.1740_1741insT	NP_001180424.1:p.Lys581Ter
NM_015840.3:c.2547_2548insT	NP_056655.2:p.Lys850Ter
NM_015841.3:c.2490_2491insT	NP_056656.2:p.Lys831Ter
XM_006711109.1:c.2655_2656insT	XP_006711172.1:p.Lys886Ter
XM_006711111.2:c.1740_1741insT	XP_006711174.1:p.Lys581Ter
XM_006711112.1:c.1740_1741insT	XP_006711175.1:p.Lys581Ter
XM_006711113.1:c.1740_1741insT	XP_006711176.1:p.Lys581Ter
XM_011509060.1:c.2754_2755insT	XP_011507362.1:p.Lys919Ter
XM_011509061.1:c.2676_2677insT	XP_011507363.1:p.Lys893Ter
XM_011509062.1:c.2643_2644insT	XP_011507364.1:p.Lys882Ter
NM_001025107.3:c.1740_1741insT	NP_001020278.1:p.Lys581Ter
NM_001111.5:c.2625_2626insT MANE Select	NP_001102.3:p.Lys876Ter
NM_001193495.2:c.1740_1741insT	NP_001180424.1:p.Lys581Ter
NM_001365045.1:c.2652_2653insT	NP_001351974.1:p.Lys885Ter
NM_001365046.1:c.1740_1741insT	NP_001351975.1:p.Lys581Ter
NM_001365047.1:c.1740_1741insT	NP_001351976.1:p.Lys581Ter
NM_001365048.1:c.1740_1741insT	NP_001351977.1:p.Lys581Ter
NM_001365049.1:c.1662_1663insT	NP_001351978.1:p.Lys555Ter
NM_015840.4:c.2547_2548insT	NP_056655.3:p.Lys850Ter
NM_015841.4:c.2490_2491insT	NP_056656.3:p.Lys831Ter
XM_006711113.2:c.1740_1741insT	XP_006711176.1:p.Lys581Ter
XM_011509061.2:c.1662_1663insT	XP_011507363.2:p.Lys555Ter
XM_024449674.1:c.2754_2755insT	XP_024305442.1:p.Lys919Ter