Canonical Allele Identifier: CA342634441

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557299A>C (hg19) ; chr1:g.154584823A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584823A>C , CM000663.2:g.154584823A>C	GRCh38
NC_000001.10:g.154557299A>C , CM000663.1:g.154557299A>C	GRCh37
NC_000001.9:g.152823923A>C	NCBI36
NG_011844.1:g.48139T>G
NG_011844.2:g.51738T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3558T>G	ENSP00000497790.2:n.3558T>G
ENST00000649724.2:c.3694T>G	ENSP00000497932.2:p.Tyr1232Asp
ENST00000680270.2:c.3547T>G	ENSP00000505532.2:p.Tyr1183Asp
ENST00000681056.2:c.3316T>G	ENSP00000506234.2:p.Tyr1106Asp
ENST00000368471.8:c.2779T>G	ENSP00000357456.3:p.Tyr927Asp
ENST00000368474.9:c.3664T>G MANE Select	ENSP00000357459.4:p.Tyr1222Asp
ENST00000492630.2:n.2457T>G
ENST00000529168.2:c.3586T>G	ENSP00000431794.2:p.Tyr1196Asp
ENST00000647682.2:n.3649T>G
ENST00000648231.2:c.2779T>G	ENSP00000497555.1:p.Tyr927Asp
ENST00000648311.1:c.2779T>G	ENSP00000498137.1:p.Tyr927Asp
ENST00000648714.2:c.*1139T>G	ENSP00000497434.2:n.*1139T>G
ENST00000649021.1:n.4400T>G
ENST00000649022.2:c.2779T>G	ENSP00000496896.2:p.Tyr927Asp
ENST00000649042.1:c.2779T>G	ENSP00000497790.1:p.Tyr927Asp
ENST00000649408.2:c.*830T>G	ENSP00000497386.2:n.*830T>G
ENST00000649724.1:c.2779T>G	ENSP00000497932.1:p.Tyr927Asp
ENST00000649749.1:c.2779T>G	ENSP00000497210.1:p.Tyr927Asp
ENST00000679375.1:c.*1896T>G	ENSP00000505887.1:n.*1896T>G
ENST00000679465.1:n.4525T>G
ENST00000679805.1:n.4400T>G
ENST00000679899.1:c.2722T>G	ENSP00000505996.1:p.Tyr908Asp
ENST00000680270.1:c.2779T>G	ENSP00000505532.1:p.Tyr927Asp
ENST00000680305.1:c.3481T>G	ENSP00000506312.1:p.Tyr1161Asp
ENST00000681056.1:c.2779T>G	ENSP00000506234.1:p.Tyr927Asp
ENST00000681235.1:c.*3186T>G	ENSP00000506606.1:n.*3186T>G
ENST00000681429.1:n.3332T>G
ENST00000681683.1:c.2779T>G	ENSP00000506666.1:p.Tyr927Asp
ENST00000681786.1:n.4525T>G
ENST00000681901.1:c.*3264T>G	ENSP00000504883.1:n.*3264T>G
ENST00000368471.7:c.2779T>G	ENSP00000357456.3:p.Tyr927Asp
ENST00000368474.8:c.3664T>G	ENSP00000357459.4:p.Tyr1222Asp
ENST00000492630.1:n.423T>G
ENST00000529168.1:c.3571T>G	ENSP00000431794.1:p.Tyr1191Asp
NM_001025107.2:c.2779T>G	NP_001020278.1:p.Tyr927Asp
NM_001111.4:c.3664T>G	NP_001102.2:p.Tyr1222Asp
NM_001193495.1:c.2779T>G	NP_001180424.1:p.Tyr927Asp
NM_015840.3:c.3586T>G	NP_056655.2:p.Tyr1196Asp
NM_015841.3:c.3529T>G	NP_056656.2:p.Tyr1177Asp
XM_006711109.1:c.3694T>G	XP_006711172.1:p.Tyr1232Asp
XM_006711111.2:c.2779T>G	XP_006711174.1:p.Tyr927Asp
XM_006711112.1:c.2779T>G	XP_006711175.1:p.Tyr927Asp
XM_006711113.1:c.2779T>G	XP_006711176.1:p.Tyr927Asp
XM_011509060.1:c.3793T>G	XP_011507362.1:p.Tyr1265Asp
XM_011509061.1:c.3715T>G	XP_011507363.1:p.Tyr1239Asp
XM_011509062.1:c.3682T>G	XP_011507364.1:p.Tyr1228Asp
NM_001025107.3:c.2779T>G	NP_001020278.1:p.Tyr927Asp
NM_001111.5:c.3664T>G MANE Select	NP_001102.3:p.Tyr1222Asp
NM_001193495.2:c.2779T>G	NP_001180424.1:p.Tyr927Asp
NM_001365045.1:c.3691T>G	NP_001351974.1:p.Tyr1231Asp
NM_001365046.1:c.2779T>G	NP_001351975.1:p.Tyr927Asp
NM_001365047.1:c.2779T>G	NP_001351976.1:p.Tyr927Asp
NM_001365048.1:c.2779T>G	NP_001351977.1:p.Tyr927Asp
NM_001365049.1:c.2701T>G	NP_001351978.1:p.Tyr901Asp
NM_015840.4:c.3586T>G	NP_056655.3:p.Tyr1196Asp
NM_015841.4:c.3529T>G	NP_056656.3:p.Tyr1177Asp
XM_006711113.2:c.2779T>G	XP_006711176.1:p.Tyr927Asp
XM_011509061.2:c.2701T>G	XP_011507363.2:p.Tyr901Asp
XM_024449674.1:c.3793T>G	XP_024305442.1:p.Tyr1265Asp