Canonical Allele Identifier: CA1139853288

Gene: ADAR CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154583949G= , CM000663.2:g.154583949G=	GRCh38
NC_000001.10:g.154556425G= , CM000663.1:g.154556425G=	GRCh37
NC_000001.9:g.152823049G=	NCBI36
NG_011844.1:g.49013C=
NG_011844.2:g.52612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.4432C= (ADAR)	ENSP00000497790.2:n.4432C=
ENST00000649724.2:c.*857C= (ADAR)	ENSP00000497932.2:n.*857C=
ENST00000680270.2:c.4421C= (ADAR)	ENSP00000505532.2:n.4421C=
ENST00000681056.2:c.*857C= (ADAR)	ENSP00000506234.2:n.*857C=
ENST00000368471.8:c.*857C= (ADAR)	ENSP00000357456.3:n.*857C=
ENST00000368474.9:c.*857C= (ADAR) MANE Select	ENSP00000357459.4:n.*857C=
ENST00000492630.2:n.3331C= (ADAR)
ENST00000529168.2:c.*857C= (ADAR)	ENSP00000431794.2:n.*857C=
ENST00000647682.2:n.4523C= (ADAR)
ENST00000648231.2:c.*857C= (ADAR)	ENSP00000497555.1:n.*857C=
ENST00000648311.1:c.*857C= (ADAR)	ENSP00000498137.1:n.*857C=
ENST00000648714.2:c.*2013C= (ADAR)	ENSP00000497434.2:n.*2013C=
ENST00000649021.1:n.5274C= (ADAR)
ENST00000649022.2:c.*857C= (ADAR)	ENSP00000496896.2:n.*857C=
ENST00000649042.1:c.*857C= (ADAR)	ENSP00000497790.1:n.*857C=
ENST00000649408.2:c.*1704C= (ADAR)	ENSP00000497386.2:n.*1704C=
ENST00000649724.1:c.*857C= (ADAR)	ENSP00000497932.1:n.*857C=
ENST00000649749.1:c.*857C= (ADAR)	ENSP00000497210.1:n.*857C=
ENST00000679375.1:c.*2770C= (ADAR)	ENSP00000505887.1:n.*2770C=
ENST00000679465.1:n.5399C= (ADAR)
ENST00000679805.1:n.5274C= (ADAR)
ENST00000679899.1:c.*857C= (ADAR)	ENSP00000505996.1:n.*857C=
ENST00000680270.1:c.*857C= (ADAR)	ENSP00000505532.1:n.*857C=
ENST00000680305.1:c.*857C= (ADAR)	ENSP00000506312.1:n.*857C=
ENST00000681056.1:c.*857C= (ADAR)	ENSP00000506234.1:n.*857C=
ENST00000681235.1:c.*4060C= (ADAR)	ENSP00000506606.1:n.*4060C=
ENST00000681429.1:n.4206C= (ADAR)
ENST00000681786.1:n.5399C= (ADAR)
ENST00000681901.1:c.*4138C= (ADAR)	ENSP00000504883.1:n.*4138C=
ENST00000368471.7:c.*857C= (ADAR)	ENSP00000357456.3:n.*857C=
ENST00000368474.8:c.*857C= (ADAR)	ENSP00000357459.4:n.*857C=
NM_001025107.2:c.*857C= (ADAR)	NP_001020278.1:n.*857C=
NM_001111.4:c.*857C= (ADAR)	NP_001102.2:n.*857C=
NM_001193495.1:c.*857C= (ADAR)	NP_001180424.1:n.*857C=
NM_015840.3:c.*857C= (ADAR)	NP_056655.2:n.*857C=
NM_015841.3:c.*857C= (ADAR)	NP_056656.2:n.*857C=
XM_006711109.1:c.*857C= (ADAR)	XP_006711172.1:n.*857C=
XM_006711111.2:c.*857C= (ADAR)	XP_006711174.1:n.*857C=
XM_006711112.1:c.*857C= (ADAR)	XP_006711175.1:n.*857C=
XM_006711113.1:c.*857C= (ADAR)	XP_006711176.1:n.*857C=
XM_011509060.1:c.*857C= (ADAR)	XP_011507362.1:n.*857C=
XM_011509061.1:c.*857C= (ADAR)	XP_011507363.1:n.*857C=
XM_011509062.1:c.*857C= (ADAR)	XP_011507364.1:n.*857C=
NM_001025107.3:c.*857C= (ADAR)	NP_001020278.1:n.*857C=
NM_001111.5:c.*857C= (ADAR) MANE Select	NP_001102.3:n.*857C=
NM_001193495.2:c.*857C= (ADAR)	NP_001180424.1:n.*857C=
NM_001365045.1:c.*857C= (ADAR)	NP_001351974.1:n.*857C=
NM_001365046.1:c.*857C= (ADAR)	NP_001351975.1:n.*857C=
NM_001365047.1:c.*857C= (ADAR)	NP_001351976.1:n.*857C=
NM_001365048.1:c.*857C= (ADAR)	NP_001351977.1:n.*857C=
NM_001365049.1:c.*857C= (ADAR)	NP_001351978.1:n.*857C=
NM_015840.4:c.*857C= (ADAR)	NP_056655.3:n.*857C=
NM_015841.4:c.*857C= (ADAR)	NP_056656.3:n.*857C=
XM_006711113.2:c.*857C= (ADAR)	XP_006711176.1:n.*857C=
XM_011509061.2:c.*857C= (ADAR)	XP_011507363.2:n.*857C=
XM_017000180.2:c.*8017G= (CHRNB2)	XP_016855669.1:n.*8017G=
XM_024449674.1:c.*857C= (ADAR)	XP_024305442.1:n.*857C=
XR_001736952.2:n.8964G= (CHRNB2)