Canonical Allele Identifier: CA2480933205

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589784T= , CM000663.2:g.154589784T=	GRCh38
NC_000001.10:g.154562260T= , CM000663.1:g.154562260T=	GRCh37
NC_000001.9:g.152828884T=	NCBI36
NG_011844.1:g.43178A=
NG_011844.2:g.46777A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2535A=	ENSP00000497790.2:n.2535A=
ENST00000649724.2:c.2671A=	ENSP00000497932.2:p.Met891=
ENST00000680270.2:c.2524A=	ENSP00000505532.2:p.Met842=
ENST00000681056.2:c.2293A=	ENSP00000506234.2:p.Met765=
ENST00000368471.8:c.1756A=	ENSP00000357456.3:p.Met586=
ENST00000368474.9:c.2641A= MANE Select	ENSP00000357459.4:p.Met881=
ENST00000529168.2:c.2563A=	ENSP00000431794.2:p.Met855=
ENST00000647682.2:n.2626A=
ENST00000648231.2:c.1756A=	ENSP00000497555.1:p.Met586=
ENST00000648311.1:c.1756A=	ENSP00000498137.1:p.Met586=
ENST00000648714.2:c.*116A=	ENSP00000497434.2:n.*116A=
ENST00000649021.1:n.2677A=
ENST00000649022.2:c.1756A=	ENSP00000496896.2:p.Met586=
ENST00000649042.1:c.1756A=	ENSP00000497790.1:p.Met586=
ENST00000649408.2:c.2641A=	ENSP00000497386.2:p.Met881=
ENST00000649724.1:c.1756A=	ENSP00000497932.1:p.Met586=
ENST00000649749.1:c.1756A=	ENSP00000497210.1:p.Met586=
ENST00000679375.1:c.*873A=	ENSP00000505887.1:n.*873A=
ENST00000679465.1:n.3094A=
ENST00000679805.1:n.2677A=
ENST00000679899.1:c.1699A=	ENSP00000505996.1:p.Met567=
ENST00000680270.1:c.1756A=	ENSP00000505532.1:p.Met586=
ENST00000680305.1:c.2641A=	ENSP00000506312.1:p.Met881=
ENST00000681056.1:c.1756A=	ENSP00000506234.1:p.Met586=
ENST00000681235.1:c.*2163A=	ENSP00000506606.1:n.*2163A=
ENST00000681429.1:n.1901A=
ENST00000681683.1:c.1756A=	ENSP00000506666.1:p.Met586=
ENST00000681786.1:n.3094A=
ENST00000681901.1:c.*2241A=	ENSP00000504883.1:n.*2241A=
ENST00000368471.7:c.1756A=	ENSP00000357456.3:p.Met586=
ENST00000368474.8:c.2641A=	ENSP00000357459.4:p.Met881=
ENST00000529168.1:c.2548A=	ENSP00000431794.1:p.Met850=
NM_001025107.2:c.1756A=	NP_001020278.1:p.Met586=
NM_001111.4:c.2641A=	NP_001102.2:p.Met881=
NM_001193495.1:c.1756A=	NP_001180424.1:p.Met586=
NM_015840.3:c.2563A=	NP_056655.2:p.Met855=
NM_015841.3:c.2506A=	NP_056656.2:p.Met836=
XM_006711109.1:c.2671A=	XP_006711172.1:p.Met891=
XM_006711111.2:c.1756A=	XP_006711174.1:p.Met586=
XM_006711112.1:c.1756A=	XP_006711175.1:p.Met586=
XM_006711113.1:c.1756A=	XP_006711176.1:p.Met586=
XM_011509060.1:c.2770A=	XP_011507362.1:p.Met924=
XM_011509061.1:c.2692A=	XP_011507363.1:p.Met898=
XM_011509062.1:c.2659A=	XP_011507364.1:p.Met887=
NM_001025107.3:c.1756A=	NP_001020278.1:p.Met586=
NM_001111.5:c.2641A= MANE Select	NP_001102.3:p.Met881=
NM_001193495.2:c.1756A=	NP_001180424.1:p.Met586=
NM_001365045.1:c.2668A=	NP_001351974.1:p.Met890=
NM_001365046.1:c.1756A=	NP_001351975.1:p.Met586=
NM_001365047.1:c.1756A=	NP_001351976.1:p.Met586=
NM_001365048.1:c.1756A=	NP_001351977.1:p.Met586=
NM_001365049.1:c.1678A=	NP_001351978.1:p.Met560=
NM_015840.4:c.2563A=	NP_056655.3:p.Met855=
NM_015841.4:c.2506A=	NP_056656.3:p.Met836=
XM_006711113.2:c.1756A=	XP_006711176.1:p.Met586=
XM_011509061.2:c.1678A=	XP_011507363.2:p.Met560=
XM_024449674.1:c.2770A=	XP_024305442.1:p.Met924=