Canonical Allele Identifier: CA2480932529

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588199T= , CM000663.2:g.154588199T=	GRCh38
NC_000001.10:g.154560675T= , CM000663.1:g.154560675T=	GRCh37
NC_000001.9:g.152827299T=	NCBI36
NG_011844.1:g.44763A=
NG_011844.2:g.48362A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2839A=	ENSP00000497790.2:n.2839A=
ENST00000649724.2:c.2975A=	ENSP00000497932.2:p.Glu992=
ENST00000680270.2:c.2828A=	ENSP00000505532.2:p.Glu943=
ENST00000681056.2:c.2597A=	ENSP00000506234.2:p.Glu866=
ENST00000368471.8:c.2060A=	ENSP00000357456.3:p.Glu687=
ENST00000368474.9:c.2945A= MANE Select	ENSP00000357459.4:p.Glu982=
ENST00000529168.2:c.2867A=	ENSP00000431794.2:p.Glu956=
ENST00000647682.2:n.2930A=
ENST00000648231.2:c.2060A=	ENSP00000497555.1:p.Glu687=
ENST00000648311.1:c.2060A=	ENSP00000498137.1:p.Glu687=
ENST00000648714.2:c.*420A=	ENSP00000497434.2:n.*420A=
ENST00000649021.1:n.3273A=
ENST00000649022.2:c.2060A=	ENSP00000496896.2:p.Glu687=
ENST00000649042.1:c.2060A=	ENSP00000497790.1:p.Glu687=
ENST00000649408.2:c.2945A=	ENSP00000497386.2:p.Glu982=
ENST00000649724.1:c.2060A=	ENSP00000497932.1:p.Glu687=
ENST00000649749.1:c.2060A=	ENSP00000497210.1:p.Glu687=
ENST00000679375.1:c.*1177A=	ENSP00000505887.1:n.*1177A=
ENST00000679465.1:n.3398A=
ENST00000679805.1:n.3273A=
ENST00000679899.1:c.2003A=	ENSP00000505996.1:p.Glu668=
ENST00000680270.1:c.2060A=	ENSP00000505532.1:p.Glu687=
ENST00000680305.1:c.2945A=	ENSP00000506312.1:p.Glu982=
ENST00000681056.1:c.2060A=	ENSP00000506234.1:p.Glu687=
ENST00000681235.1:c.*2467A=	ENSP00000506606.1:n.*2467A=
ENST00000681429.1:n.2205A=
ENST00000681683.1:c.2060A=	ENSP00000506666.1:p.Glu687=
ENST00000681786.1:n.3398A=
ENST00000681901.1:c.*2545A=	ENSP00000504883.1:n.*2545A=
ENST00000368471.7:c.2060A=	ENSP00000357456.3:p.Glu687=
ENST00000368474.8:c.2945A=	ENSP00000357459.4:p.Glu982=
ENST00000529168.1:c.2852A=	ENSP00000431794.1:p.Glu951=
ENST00000530954.1:n.82A=
ENST00000534279.1:n.404A=
NM_001025107.2:c.2060A=	NP_001020278.1:p.Glu687=
NM_001111.4:c.2945A=	NP_001102.2:p.Glu982=
NM_001193495.1:c.2060A=	NP_001180424.1:p.Glu687=
NM_015840.3:c.2867A=	NP_056655.2:p.Glu956=
NM_015841.3:c.2810A=	NP_056656.2:p.Glu937=
XM_006711109.1:c.2975A=	XP_006711172.1:p.Glu992=
XM_006711111.2:c.2060A=	XP_006711174.1:p.Glu687=
XM_006711112.1:c.2060A=	XP_006711175.1:p.Glu687=
XM_006711113.1:c.2060A=	XP_006711176.1:p.Glu687=
XM_011509060.1:c.3074A=	XP_011507362.1:p.Glu1025=
XM_011509061.1:c.2996A=	XP_011507363.1:p.Glu999=
XM_011509062.1:c.2963A=	XP_011507364.1:p.Glu988=
NM_001025107.3:c.2060A=	NP_001020278.1:p.Glu687=
NM_001111.5:c.2945A= MANE Select	NP_001102.3:p.Glu982=
NM_001193495.2:c.2060A=	NP_001180424.1:p.Glu687=
NM_001365045.1:c.2972A=	NP_001351974.1:p.Glu991=
NM_001365046.1:c.2060A=	NP_001351975.1:p.Glu687=
NM_001365047.1:c.2060A=	NP_001351976.1:p.Glu687=
NM_001365048.1:c.2060A=	NP_001351977.1:p.Glu687=
NM_001365049.1:c.1982A=	NP_001351978.1:p.Glu661=
NM_015840.4:c.2867A=	NP_056655.3:p.Glu956=
NM_015841.4:c.2810A=	NP_056656.3:p.Glu937=
XM_006711113.2:c.2060A=	XP_006711176.1:p.Glu687=
XM_011509061.2:c.1982A=	XP_011507363.2:p.Glu661=
XM_024449674.1:c.3074A=	XP_024305442.1:p.Glu1025=