Canonical Allele Identifier: CA2586963875

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589779_154589780dup , CM000663.2:g.154589779_154589780dup	GRCh38
NC_000001.10:g.154562255_154562256dup , CM000663.1:g.154562255_154562256dup	GRCh37
NC_000001.9:g.152828879_152828880dup	NCBI36
NG_011844.1:g.43184_43185dup
NG_011844.2:g.46783_46784dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2541_2542dup	ENSP00000497790.2:n.2541_2542dup
ENST00000649724.2:c.2677_2678dup	ENSP00000497932.2:p.Val894SerfsTer12
ENST00000680270.2:c.2530_2531dup	ENSP00000505532.2:p.Val845SerfsTer12
ENST00000681056.2:c.2299_2300dup	ENSP00000506234.2:p.Val768SerfsTer12
ENST00000368471.8:c.1762_1763dup	ENSP00000357456.3:p.Val589SerfsTer12
ENST00000368474.9:c.2647_2648dup MANE Select	ENSP00000357459.4:p.Val884SerfsTer12
ENST00000529168.2:c.2569_2570dup	ENSP00000431794.2:p.Val858SerfsTer12
ENST00000647682.2:n.2632_2633dup
ENST00000648231.2:c.1762_1763dup	ENSP00000497555.1:p.Val589SerfsTer12
ENST00000648311.1:c.1762_1763dup	ENSP00000498137.1:p.Val589SerfsTer12
ENST00000648714.2:c.*122_*123dup	ENSP00000497434.2:n.*122_*123dup
ENST00000649021.1:n.2683_2684dup
ENST00000649022.2:c.1762_1763dup	ENSP00000496896.2:p.Val589SerfsTer12
ENST00000649042.1:c.1762_1763dup	ENSP00000497790.1:p.Val589SerfsTer12
ENST00000649408.2:c.2647_2648dup	ENSP00000497386.2:p.Val884SerfsTer12
ENST00000649724.1:c.1762_1763dup	ENSP00000497932.1:p.Val589SerfsTer12
ENST00000649749.1:c.1762_1763dup	ENSP00000497210.1:p.Val589SerfsTer12
ENST00000679375.1:c.*879_*880dup	ENSP00000505887.1:n.*879_*880dup
ENST00000679465.1:n.3100_3101dup
ENST00000679805.1:n.2683_2684dup
ENST00000679899.1:c.1705_1706dup	ENSP00000505996.1:p.Val570SerfsTer12
ENST00000680270.1:c.1762_1763dup	ENSP00000505532.1:p.Val589SerfsTer12
ENST00000680305.1:c.2647_2648dup	ENSP00000506312.1:p.Val884SerfsTer12
ENST00000681056.1:c.1762_1763dup	ENSP00000506234.1:p.Val589SerfsTer12
ENST00000681235.1:c.*2169_*2170dup	ENSP00000506606.1:n.*2169_*2170dup
ENST00000681429.1:n.1907_1908dup
ENST00000681683.1:c.1762_1763dup	ENSP00000506666.1:p.Val589SerfsTer12
ENST00000681786.1:n.3100_3101dup
ENST00000681901.1:c.*2247_*2248dup	ENSP00000504883.1:n.*2247_*2248dup
ENST00000368471.7:c.1762_1763dup	ENSP00000357456.3:p.Val589SerfsTer12
ENST00000368474.8:c.2647_2648dup	ENSP00000357459.4:p.Val884SerfsTer12
ENST00000529168.1:c.2554_2555dup	ENSP00000431794.1:p.Val853SerfsTer12
NM_001025107.2:c.1762_1763dup	NP_001020278.1:p.Val589SerfsTer12
NM_001111.4:c.2647_2648dup	NP_001102.2:p.Val884SerfsTer12
NM_001193495.1:c.1762_1763dup	NP_001180424.1:p.Val589SerfsTer12
NM_015840.3:c.2569_2570dup	NP_056655.2:p.Val858SerfsTer12
NM_015841.3:c.2512_2513dup	NP_056656.2:p.Val839SerfsTer12
XM_006711109.1:c.2677_2678dup	XP_006711172.1:p.Val894SerfsTer12
XM_006711111.2:c.1762_1763dup	XP_006711174.1:p.Val589SerfsTer12
XM_006711112.1:c.1762_1763dup	XP_006711175.1:p.Val589SerfsTer12
XM_006711113.1:c.1762_1763dup	XP_006711176.1:p.Val589SerfsTer12
XM_011509060.1:c.2776_2777dup	XP_011507362.1:p.Val927SerfsTer12
XM_011509061.1:c.2698_2699dup	XP_011507363.1:p.Val901SerfsTer12
XM_011509062.1:c.2665_2666dup	XP_011507364.1:p.Val890SerfsTer12
NM_001025107.3:c.1762_1763dup	NP_001020278.1:p.Val589SerfsTer12
NM_001111.5:c.2647_2648dup MANE Select	NP_001102.3:p.Val884SerfsTer12
NM_001193495.2:c.1762_1763dup	NP_001180424.1:p.Val589SerfsTer12
NM_001365045.1:c.2674_2675dup	NP_001351974.1:p.Val893SerfsTer12
NM_001365046.1:c.1762_1763dup	NP_001351975.1:p.Val589SerfsTer12
NM_001365047.1:c.1762_1763dup	NP_001351976.1:p.Val589SerfsTer12
NM_001365048.1:c.1762_1763dup	NP_001351977.1:p.Val589SerfsTer12
NM_001365049.1:c.1684_1685dup	NP_001351978.1:p.Val563SerfsTer12
NM_015840.4:c.2569_2570dup	NP_056655.3:p.Val858SerfsTer12
NM_015841.4:c.2512_2513dup	NP_056656.3:p.Val839SerfsTer12
XM_006711113.2:c.1762_1763dup	XP_006711176.1:p.Val589SerfsTer12
XM_011509061.2:c.1684_1685dup	XP_011507363.2:p.Val563SerfsTer12
XM_024449674.1:c.2776_2777dup	XP_024305442.1:p.Val927SerfsTer12