Canonical Allele Identifier: CA420974650

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585765G>A , CM000663.2:g.154585765G>A	GRCh38
NC_000001.10:g.154558241G>A , CM000663.1:g.154558241G>A	GRCh37
NC_000001.9:g.152824865G>A	NCBI36
NG_011844.1:g.47197C>T
NG_011844.2:g.50796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3197C>T	ENSP00000497790.2:n.3197C>T
ENST00000649724.2:c.3333C>T	ENSP00000497932.2:p.Val1111=
ENST00000680270.2:c.3186C>T	ENSP00000505532.2:p.Val1062=
ENST00000681056.2:c.2955C>T	ENSP00000506234.2:p.Val985=
ENST00000368471.8:c.2418C>T	ENSP00000357456.3:p.Val806=
ENST00000368474.9:c.3303C>T MANE Select	ENSP00000357459.4:p.Val1101=
ENST00000492630.2:n.1688C>T
ENST00000529168.2:c.3225C>T	ENSP00000431794.2:p.Val1075=
ENST00000647682.2:n.3288C>T
ENST00000648231.2:c.2418C>T	ENSP00000497555.1:p.Val806=
ENST00000648311.1:c.2418C>T	ENSP00000498137.1:p.Val806=
ENST00000648714.2:c.*778C>T	ENSP00000497434.2:n.*778C>T
ENST00000649021.1:n.3631C>T
ENST00000649022.2:c.2418C>T	ENSP00000496896.2:p.Val806=
ENST00000649042.1:c.2418C>T	ENSP00000497790.1:p.Val806=
ENST00000649408.2:c.*469C>T	ENSP00000497386.2:n.*469C>T
ENST00000649724.1:c.2418C>T	ENSP00000497932.1:p.Val806=
ENST00000649749.1:c.2418C>T	ENSP00000497210.1:p.Val806=
ENST00000679375.1:c.*1535C>T	ENSP00000505887.1:n.*1535C>T
ENST00000679465.1:n.3756C>T
ENST00000679805.1:n.3631C>T
ENST00000679899.1:c.2361C>T	ENSP00000505996.1:p.Val787=
ENST00000680270.1:c.2418C>T	ENSP00000505532.1:p.Val806=
ENST00000680305.1:c.3120C>T	ENSP00000506312.1:p.Val1040=
ENST00000681056.1:c.2418C>T	ENSP00000506234.1:p.Val806=
ENST00000681235.1:c.*2825C>T	ENSP00000506606.1:n.*2825C>T
ENST00000681429.1:n.2563C>T
ENST00000681683.1:c.2418C>T	ENSP00000506666.1:p.Val806=
ENST00000681786.1:n.3756C>T
ENST00000681901.1:c.*2903C>T	ENSP00000504883.1:n.*2903C>T
ENST00000368471.7:c.2418C>T	ENSP00000357456.3:p.Val806=
ENST00000368474.8:c.3303C>T	ENSP00000357459.4:p.Val1101=
ENST00000529168.1:c.3210C>T	ENSP00000431794.1:p.Val1070=
ENST00000530954.1:n.440C>T
NM_001025107.2:c.2418C>T	NP_001020278.1:p.Val806=
NM_001111.4:c.3303C>T	NP_001102.2:p.Val1101=
NM_001193495.1:c.2418C>T	NP_001180424.1:p.Val806=
NM_015840.3:c.3225C>T	NP_056655.2:p.Val1075=
NM_015841.3:c.3168C>T	NP_056656.2:p.Val1056=
XM_006711109.1:c.3333C>T	XP_006711172.1:p.Val1111=
XM_006711111.2:c.2418C>T	XP_006711174.1:p.Val806=
XM_006711112.1:c.2418C>T	XP_006711175.1:p.Val806=
XM_006711113.1:c.2418C>T	XP_006711176.1:p.Val806=
XM_011509060.1:c.3432C>T	XP_011507362.1:p.Val1144=
XM_011509061.1:c.3354C>T	XP_011507363.1:p.Val1118=
XM_011509062.1:c.3321C>T	XP_011507364.1:p.Val1107=
NM_001025107.3:c.2418C>T	NP_001020278.1:p.Val806=
NM_001111.5:c.3303C>T MANE Select	NP_001102.3:p.Val1101=
NM_001193495.2:c.2418C>T	NP_001180424.1:p.Val806=
NM_001365045.1:c.3330C>T	NP_001351974.1:p.Val1110=
NM_001365046.1:c.2418C>T	NP_001351975.1:p.Val806=
NM_001365047.1:c.2418C>T	NP_001351976.1:p.Val806=
NM_001365048.1:c.2418C>T	NP_001351977.1:p.Val806=
NM_001365049.1:c.2340C>T	NP_001351978.1:p.Val780=
NM_015840.4:c.3225C>T	NP_056655.3:p.Val1075=
NM_015841.4:c.3168C>T	NP_056656.3:p.Val1056=
XM_006711113.2:c.2418C>T	XP_006711176.1:p.Val806=
XM_011509061.2:c.2340C>T	XP_011507363.2:p.Val780=
XM_024449674.1:c.3432C>T	XP_024305442.1:p.Val1144=