Canonical Allele Identifier: CA1140495917

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584993A= , CM000663.2:g.154584993A=	GRCh38
NC_000001.10:g.154557469A= , CM000663.1:g.154557469A=	GRCh37
NC_000001.9:g.152824093A=	NCBI36
NG_011844.1:g.47969T=
NG_011844.2:g.51568T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3388T=	ENSP00000497790.2:n.3388T=
ENST00000649724.2:c.3524T=	ENSP00000497932.2:p.Phe1175=
ENST00000680270.2:c.3377T=	ENSP00000505532.2:p.Phe1126=
ENST00000681056.2:c.3146T=	ENSP00000506234.2:p.Phe1049=
ENST00000368471.8:c.2609T=	ENSP00000357456.3:p.Phe870=
ENST00000368474.9:c.3494T= MANE Select	ENSP00000357459.4:p.Phe1165=
ENST00000492630.2:n.2287T=
ENST00000529168.2:c.3416T=	ENSP00000431794.2:p.Phe1139=
ENST00000647682.2:n.3479T=
ENST00000648231.2:c.2609T=	ENSP00000497555.1:p.Phe870=
ENST00000648311.1:c.2609T=	ENSP00000498137.1:p.Phe870=
ENST00000648714.2:c.*969T=	ENSP00000497434.2:n.*969T=
ENST00000649021.1:n.4230T=
ENST00000649022.2:c.2609T=	ENSP00000496896.2:p.Phe870=
ENST00000649042.1:c.2609T=	ENSP00000497790.1:p.Phe870=
ENST00000649408.2:c.*660T=	ENSP00000497386.2:n.*660T=
ENST00000649724.1:c.2609T=	ENSP00000497932.1:p.Phe870=
ENST00000649749.1:c.2609T=	ENSP00000497210.1:p.Phe870=
ENST00000679375.1:c.*1726T=	ENSP00000505887.1:n.*1726T=
ENST00000679465.1:n.4355T=
ENST00000679805.1:n.4230T=
ENST00000679899.1:c.2552T=	ENSP00000505996.1:p.Phe851=
ENST00000680270.1:c.2609T=	ENSP00000505532.1:p.Phe870=
ENST00000680305.1:c.3311T=	ENSP00000506312.1:p.Phe1104=
ENST00000681056.1:c.2609T=	ENSP00000506234.1:p.Phe870=
ENST00000681235.1:c.*3016T=	ENSP00000506606.1:n.*3016T=
ENST00000681429.1:n.3162T=
ENST00000681683.1:c.2609T=	ENSP00000506666.1:p.Phe870=
ENST00000681786.1:n.4355T=
ENST00000681901.1:c.*3094T=	ENSP00000504883.1:n.*3094T=
ENST00000368471.7:c.2609T=	ENSP00000357456.3:p.Phe870=
ENST00000368474.8:c.3494T=	ENSP00000357459.4:p.Phe1165=
ENST00000492630.1:n.253T=
ENST00000529168.1:c.3401T=	ENSP00000431794.1:p.Phe1134=
NM_001025107.2:c.2609T=	NP_001020278.1:p.Phe870=
NM_001111.4:c.3494T=	NP_001102.2:p.Phe1165=
NM_001193495.1:c.2609T=	NP_001180424.1:p.Phe870=
NM_015840.3:c.3416T=	NP_056655.2:p.Phe1139=
NM_015841.3:c.3359T=	NP_056656.2:p.Phe1120=
XM_006711109.1:c.3524T=	XP_006711172.1:p.Phe1175=
XM_006711111.2:c.2609T=	XP_006711174.1:p.Phe870=
XM_006711112.1:c.2609T=	XP_006711175.1:p.Phe870=
XM_006711113.1:c.2609T=	XP_006711176.1:p.Phe870=
XM_011509060.1:c.3623T=	XP_011507362.1:p.Phe1208=
XM_011509061.1:c.3545T=	XP_011507363.1:p.Phe1182=
XM_011509062.1:c.3512T=	XP_011507364.1:p.Phe1171=
NM_001025107.3:c.2609T=	NP_001020278.1:p.Phe870=
NM_001111.5:c.3494T= MANE Select	NP_001102.3:p.Phe1165=
NM_001193495.2:c.2609T=	NP_001180424.1:p.Phe870=
NM_001365045.1:c.3521T=	NP_001351974.1:p.Phe1174=
NM_001365046.1:c.2609T=	NP_001351975.1:p.Phe870=
NM_001365047.1:c.2609T=	NP_001351976.1:p.Phe870=
NM_001365048.1:c.2609T=	NP_001351977.1:p.Phe870=
NM_001365049.1:c.2531T=	NP_001351978.1:p.Phe844=
NM_015840.4:c.3416T=	NP_056655.3:p.Phe1139=
NM_015841.4:c.3359T=	NP_056656.3:p.Phe1120=
XM_006711113.2:c.2609T=	XP_006711176.1:p.Phe870=
XM_011509061.2:c.2531T=	XP_011507363.2:p.Phe844=
XM_024449674.1:c.3623T=	XP_024305442.1:p.Phe1208=