Canonical Allele Identifier: CA2480933211

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589797T= , CM000663.2:g.154589797T=	GRCh38
NC_000001.10:g.154562273T= , CM000663.1:g.154562273T=	GRCh37
NC_000001.9:g.152828897T=	NCBI36
NG_011844.1:g.43165A=
NG_011844.2:g.46764A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2522A=	ENSP00000497790.2:n.2522A=
ENST00000649724.2:c.2658A=	ENSP00000497932.2:p.Lys886=
ENST00000680270.2:c.2511A=	ENSP00000505532.2:p.Lys837=
ENST00000681056.2:c.2280A=	ENSP00000506234.2:p.Lys760=
ENST00000368471.8:c.1743A=	ENSP00000357456.3:p.Lys581=
ENST00000368474.9:c.2628A= MANE Select	ENSP00000357459.4:p.Lys876=
ENST00000529168.2:c.2550A=	ENSP00000431794.2:p.Lys850=
ENST00000647682.2:n.2613A=
ENST00000648231.2:c.1743A=	ENSP00000497555.1:p.Lys581=
ENST00000648311.1:c.1743A=	ENSP00000498137.1:p.Lys581=
ENST00000648714.2:c.*103A=	ENSP00000497434.2:n.*103A=
ENST00000649021.1:n.2664A=
ENST00000649022.2:c.1743A=	ENSP00000496896.2:p.Lys581=
ENST00000649042.1:c.1743A=	ENSP00000497790.1:p.Lys581=
ENST00000649408.2:c.2628A=	ENSP00000497386.2:p.Lys876=
ENST00000649724.1:c.1743A=	ENSP00000497932.1:p.Lys581=
ENST00000649749.1:c.1743A=	ENSP00000497210.1:p.Lys581=
ENST00000679375.1:c.*860A=	ENSP00000505887.1:n.*860A=
ENST00000679465.1:n.3081A=
ENST00000679805.1:n.2664A=
ENST00000679899.1:c.1686A=	ENSP00000505996.1:p.Lys562=
ENST00000680270.1:c.1743A=	ENSP00000505532.1:p.Lys581=
ENST00000680305.1:c.2628A=	ENSP00000506312.1:p.Lys876=
ENST00000681056.1:c.1743A=	ENSP00000506234.1:p.Lys581=
ENST00000681235.1:c.*2150A=	ENSP00000506606.1:n.*2150A=
ENST00000681429.1:n.1888A=
ENST00000681683.1:c.1743A=	ENSP00000506666.1:p.Lys581=
ENST00000681786.1:n.3081A=
ENST00000681901.1:c.*2228A=	ENSP00000504883.1:n.*2228A=
ENST00000368471.7:c.1743A=	ENSP00000357456.3:p.Lys581=
ENST00000368474.8:c.2628A=	ENSP00000357459.4:p.Lys876=
ENST00000529168.1:c.2535A=	ENSP00000431794.1:p.Lys845=
NM_001025107.2:c.1743A=	NP_001020278.1:p.Lys581=
NM_001111.4:c.2628A=	NP_001102.2:p.Lys876=
NM_001193495.1:c.1743A=	NP_001180424.1:p.Lys581=
NM_015840.3:c.2550A=	NP_056655.2:p.Lys850=
NM_015841.3:c.2493A=	NP_056656.2:p.Lys831=
XM_006711109.1:c.2658A=	XP_006711172.1:p.Lys886=
XM_006711111.2:c.1743A=	XP_006711174.1:p.Lys581=
XM_006711112.1:c.1743A=	XP_006711175.1:p.Lys581=
XM_006711113.1:c.1743A=	XP_006711176.1:p.Lys581=
XM_011509060.1:c.2757A=	XP_011507362.1:p.Lys919=
XM_011509061.1:c.2679A=	XP_011507363.1:p.Lys893=
XM_011509062.1:c.2646A=	XP_011507364.1:p.Lys882=
NM_001025107.3:c.1743A=	NP_001020278.1:p.Lys581=
NM_001111.5:c.2628A= MANE Select	NP_001102.3:p.Lys876=
NM_001193495.2:c.1743A=	NP_001180424.1:p.Lys581=
NM_001365045.1:c.2655A=	NP_001351974.1:p.Lys885=
NM_001365046.1:c.1743A=	NP_001351975.1:p.Lys581=
NM_001365047.1:c.1743A=	NP_001351976.1:p.Lys581=
NM_001365048.1:c.1743A=	NP_001351977.1:p.Lys581=
NM_001365049.1:c.1665A=	NP_001351978.1:p.Lys555=
NM_015840.4:c.2550A=	NP_056655.3:p.Lys850=
NM_015841.4:c.2493A=	NP_056656.3:p.Lys831=
XM_006711113.2:c.1743A=	XP_006711176.1:p.Lys581=
XM_011509061.2:c.1665A=	XP_011507363.2:p.Lys555=
XM_024449674.1:c.2757A=	XP_024305442.1:p.Lys919=