Canonical Allele Identifier: CA2480933213

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589808T= , CM000663.2:g.154589808T=	GRCh38
NC_000001.10:g.154562284T= , CM000663.1:g.154562284T=	GRCh37
NC_000001.9:g.152828908T=	NCBI36
NG_011844.1:g.43154A=
NG_011844.2:g.46753A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2511A=	ENSP00000497790.2:n.2511A=
ENST00000649724.2:c.2647A=	ENSP00000497932.2:p.Ile883=
ENST00000680270.2:c.2500A=	ENSP00000505532.2:p.Ile834=
ENST00000681056.2:c.2269A=	ENSP00000506234.2:p.Ile757=
ENST00000368471.8:c.1732A=	ENSP00000357456.3:p.Ile578=
ENST00000368474.9:c.2617A= MANE Select	ENSP00000357459.4:p.Ile873=
ENST00000529168.2:c.2539A=	ENSP00000431794.2:p.Ile847=
ENST00000647682.2:n.2602A=
ENST00000648231.2:c.1732A=	ENSP00000497555.1:p.Ile578=
ENST00000648311.1:c.1732A=	ENSP00000498137.1:p.Ile578=
ENST00000648714.2:c.*92A=	ENSP00000497434.2:n.*92A=
ENST00000649021.1:n.2653A=
ENST00000649022.2:c.1732A=	ENSP00000496896.2:p.Ile578=
ENST00000649042.1:c.1732A=	ENSP00000497790.1:p.Ile578=
ENST00000649408.2:c.2617A=	ENSP00000497386.2:p.Ile873=
ENST00000649724.1:c.1732A=	ENSP00000497932.1:p.Ile578=
ENST00000649749.1:c.1732A=	ENSP00000497210.1:p.Ile578=
ENST00000679375.1:c.*849A=	ENSP00000505887.1:n.*849A=
ENST00000679465.1:n.3070A=
ENST00000679805.1:n.2653A=
ENST00000679899.1:c.1675A=	ENSP00000505996.1:p.Ile559=
ENST00000680270.1:c.1732A=	ENSP00000505532.1:p.Ile578=
ENST00000680305.1:c.2617A=	ENSP00000506312.1:p.Ile873=
ENST00000681056.1:c.1732A=	ENSP00000506234.1:p.Ile578=
ENST00000681235.1:c.*2139A=	ENSP00000506606.1:n.*2139A=
ENST00000681429.1:n.1877A=
ENST00000681683.1:c.1732A=	ENSP00000506666.1:p.Ile578=
ENST00000681786.1:n.3070A=
ENST00000681901.1:c.*2217A=	ENSP00000504883.1:n.*2217A=
ENST00000368471.7:c.1732A=	ENSP00000357456.3:p.Ile578=
ENST00000368474.8:c.2617A=	ENSP00000357459.4:p.Ile873=
ENST00000529168.1:c.2524A=	ENSP00000431794.1:p.Ile842=
NM_001025107.2:c.1732A=	NP_001020278.1:p.Ile578=
NM_001111.4:c.2617A=	NP_001102.2:p.Ile873=
NM_001193495.1:c.1732A=	NP_001180424.1:p.Ile578=
NM_015840.3:c.2539A=	NP_056655.2:p.Ile847=
NM_015841.3:c.2482A=	NP_056656.2:p.Ile828=
XM_006711109.1:c.2647A=	XP_006711172.1:p.Ile883=
XM_006711111.2:c.1732A=	XP_006711174.1:p.Ile578=
XM_006711112.1:c.1732A=	XP_006711175.1:p.Ile578=
XM_006711113.1:c.1732A=	XP_006711176.1:p.Ile578=
XM_011509060.1:c.2746A=	XP_011507362.1:p.Ile916=
XM_011509061.1:c.2668A=	XP_011507363.1:p.Ile890=
XM_011509062.1:c.2635A=	XP_011507364.1:p.Ile879=
NM_001025107.3:c.1732A=	NP_001020278.1:p.Ile578=
NM_001111.5:c.2617A= MANE Select	NP_001102.3:p.Ile873=
NM_001193495.2:c.1732A=	NP_001180424.1:p.Ile578=
NM_001365045.1:c.2644A=	NP_001351974.1:p.Ile882=
NM_001365046.1:c.1732A=	NP_001351975.1:p.Ile578=
NM_001365047.1:c.1732A=	NP_001351976.1:p.Ile578=
NM_001365048.1:c.1732A=	NP_001351977.1:p.Ile578=
NM_001365049.1:c.1654A=	NP_001351978.1:p.Ile552=
NM_015840.4:c.2539A=	NP_056655.3:p.Ile847=
NM_015841.4:c.2482A=	NP_056656.3:p.Ile828=
XM_006711113.2:c.1732A=	XP_006711176.1:p.Ile578=
XM_011509061.2:c.1654A=	XP_011507363.2:p.Ile552=
XM_024449674.1:c.2746A=	XP_024305442.1:p.Ile916=