Canonical Allele Identifier: CA2480932546

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588254C= , CM000663.2:g.154588254C=	GRCh38
NC_000001.10:g.154560730C= , CM000663.1:g.154560730C=	GRCh37
NC_000001.9:g.152827354C=	NCBI36
NG_011844.1:g.44708G=
NG_011844.2:g.48307G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2784G=	ENSP00000497790.2:n.2784G=
ENST00000649724.2:c.2920G=	ENSP00000497932.2:p.Ala974=
ENST00000680270.2:c.2773G=	ENSP00000505532.2:p.Ala925=
ENST00000681056.2:c.2542G=	ENSP00000506234.2:p.Ala848=
ENST00000368471.8:c.2005G=	ENSP00000357456.3:p.Ala669=
ENST00000368474.9:c.2890G= MANE Select	ENSP00000357459.4:p.Ala964=
ENST00000529168.2:c.2812G=	ENSP00000431794.2:p.Ala938=
ENST00000647682.2:n.2875G=
ENST00000648231.2:c.2005G=	ENSP00000497555.1:p.Ala669=
ENST00000648311.1:c.2005G=	ENSP00000498137.1:p.Ala669=
ENST00000648714.2:c.*365G=	ENSP00000497434.2:n.*365G=
ENST00000649021.1:n.3218G=
ENST00000649022.2:c.2005G=	ENSP00000496896.2:p.Ala669=
ENST00000649042.1:c.2005G=	ENSP00000497790.1:p.Ala669=
ENST00000649408.2:c.2890G=	ENSP00000497386.2:p.Ala964=
ENST00000649724.1:c.2005G=	ENSP00000497932.1:p.Ala669=
ENST00000649749.1:c.2005G=	ENSP00000497210.1:p.Ala669=
ENST00000679375.1:c.*1122G=	ENSP00000505887.1:n.*1122G=
ENST00000679465.1:n.3343G=
ENST00000679805.1:n.3218G=
ENST00000679899.1:c.1948G=	ENSP00000505996.1:p.Ala650=
ENST00000680270.1:c.2005G=	ENSP00000505532.1:p.Ala669=
ENST00000680305.1:c.2890G=	ENSP00000506312.1:p.Ala964=
ENST00000681056.1:c.2005G=	ENSP00000506234.1:p.Ala669=
ENST00000681235.1:c.*2412G=	ENSP00000506606.1:n.*2412G=
ENST00000681429.1:n.2150G=
ENST00000681683.1:c.2005G=	ENSP00000506666.1:p.Ala669=
ENST00000681786.1:n.3343G=
ENST00000681901.1:c.*2490G=	ENSP00000504883.1:n.*2490G=
ENST00000368471.7:c.2005G=	ENSP00000357456.3:p.Ala669=
ENST00000368474.8:c.2890G=	ENSP00000357459.4:p.Ala964=
ENST00000529168.1:c.2797G=	ENSP00000431794.1:p.Ala933=
ENST00000530954.1:n.27G=
ENST00000534279.1:n.349G=
NM_001025107.2:c.2005G=	NP_001020278.1:p.Ala669=
NM_001111.4:c.2890G=	NP_001102.2:p.Ala964=
NM_001193495.1:c.2005G=	NP_001180424.1:p.Ala669=
NM_015840.3:c.2812G=	NP_056655.2:p.Ala938=
NM_015841.3:c.2755G=	NP_056656.2:p.Ala919=
XM_006711109.1:c.2920G=	XP_006711172.1:p.Ala974=
XM_006711111.2:c.2005G=	XP_006711174.1:p.Ala669=
XM_006711112.1:c.2005G=	XP_006711175.1:p.Ala669=
XM_006711113.1:c.2005G=	XP_006711176.1:p.Ala669=
XM_011509060.1:c.3019G=	XP_011507362.1:p.Ala1007=
XM_011509061.1:c.2941G=	XP_011507363.1:p.Ala981=
XM_011509062.1:c.2908G=	XP_011507364.1:p.Ala970=
NM_001025107.3:c.2005G=	NP_001020278.1:p.Ala669=
NM_001111.5:c.2890G= MANE Select	NP_001102.3:p.Ala964=
NM_001193495.2:c.2005G=	NP_001180424.1:p.Ala669=
NM_001365045.1:c.2917G=	NP_001351974.1:p.Ala973=
NM_001365046.1:c.2005G=	NP_001351975.1:p.Ala669=
NM_001365047.1:c.2005G=	NP_001351976.1:p.Ala669=
NM_001365048.1:c.2005G=	NP_001351977.1:p.Ala669=
NM_001365049.1:c.1927G=	NP_001351978.1:p.Ala643=
NM_015840.4:c.2812G=	NP_056655.3:p.Ala938=
NM_015841.4:c.2755G=	NP_056656.3:p.Ala919=
XM_006711113.2:c.2005G=	XP_006711176.1:p.Ala669=
XM_011509061.2:c.1927G=	XP_011507363.2:p.Ala643=
XM_024449674.1:c.3019G=	XP_024305442.1:p.Ala1007=