Canonical Allele Identifier: CA342635951

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154560616T>A (hg19) ; chr1:g.154588140T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588140T>A , CM000663.2:g.154588140T>A	GRCh38
NC_000001.10:g.154560616T>A , CM000663.1:g.154560616T>A	GRCh37
NC_000001.9:g.152827240T>A	NCBI36
NG_011844.1:g.44822A>T
NG_011844.2:g.48421A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2898A>T	ENSP00000497790.2:n.2898A>T
ENST00000649724.2:c.3034A>T	ENSP00000497932.2:p.Thr1012Ser
ENST00000680270.2:c.2887A>T	ENSP00000505532.2:p.Thr963Ser
ENST00000681056.2:c.2656A>T	ENSP00000506234.2:p.Thr886Ser
ENST00000368471.8:c.2119A>T	ENSP00000357456.3:p.Thr707Ser
ENST00000368474.9:c.3004A>T MANE Select	ENSP00000357459.4:p.Thr1002Ser
ENST00000529168.2:c.2926A>T	ENSP00000431794.2:p.Thr976Ser
ENST00000647682.2:n.2989A>T
ENST00000648231.2:c.2119A>T	ENSP00000497555.1:p.Thr707Ser
ENST00000648311.1:c.2119A>T	ENSP00000498137.1:p.Thr707Ser
ENST00000648714.2:c.*479A>T	ENSP00000497434.2:n.*479A>T
ENST00000649021.1:n.3332A>T
ENST00000649022.2:c.2119A>T	ENSP00000496896.2:p.Thr707Ser
ENST00000649042.1:c.2119A>T	ENSP00000497790.1:p.Thr707Ser
ENST00000649408.2:c.3004A>T	ENSP00000497386.2:p.Thr1002Ser
ENST00000649724.1:c.2119A>T	ENSP00000497932.1:p.Thr707Ser
ENST00000649749.1:c.2119A>T	ENSP00000497210.1:p.Thr707Ser
ENST00000679375.1:c.*1236A>T	ENSP00000505887.1:n.*1236A>T
ENST00000679465.1:n.3457A>T
ENST00000679805.1:n.3332A>T
ENST00000679899.1:c.2062A>T	ENSP00000505996.1:p.Thr688Ser
ENST00000680270.1:c.2119A>T	ENSP00000505532.1:p.Thr707Ser
ENST00000680305.1:c.3004A>T	ENSP00000506312.1:p.Thr1002Ser
ENST00000681056.1:c.2119A>T	ENSP00000506234.1:p.Thr707Ser
ENST00000681235.1:c.*2526A>T	ENSP00000506606.1:n.*2526A>T
ENST00000681429.1:n.2264A>T
ENST00000681683.1:c.2119A>T	ENSP00000506666.1:p.Thr707Ser
ENST00000681786.1:n.3457A>T
ENST00000681901.1:c.*2604A>T	ENSP00000504883.1:n.*2604A>T
ENST00000368471.7:c.2119A>T	ENSP00000357456.3:p.Thr707Ser
ENST00000368474.8:c.3004A>T	ENSP00000357459.4:p.Thr1002Ser
ENST00000529168.1:c.2911A>T	ENSP00000431794.1:p.Thr971Ser
ENST00000530954.1:n.141A>T
ENST00000534279.1:n.463A>T
NM_001025107.2:c.2119A>T	NP_001020278.1:p.Thr707Ser
NM_001111.4:c.3004A>T	NP_001102.2:p.Thr1002Ser
NM_001193495.1:c.2119A>T	NP_001180424.1:p.Thr707Ser
NM_015840.3:c.2926A>T	NP_056655.2:p.Thr976Ser
NM_015841.3:c.2869A>T	NP_056656.2:p.Thr957Ser
XM_006711109.1:c.3034A>T	XP_006711172.1:p.Thr1012Ser
XM_006711111.2:c.2119A>T	XP_006711174.1:p.Thr707Ser
XM_006711112.1:c.2119A>T	XP_006711175.1:p.Thr707Ser
XM_006711113.1:c.2119A>T	XP_006711176.1:p.Thr707Ser
XM_011509060.1:c.3133A>T	XP_011507362.1:p.Thr1045Ser
XM_011509061.1:c.3055A>T	XP_011507363.1:p.Thr1019Ser
XM_011509062.1:c.3022A>T	XP_011507364.1:p.Thr1008Ser
NM_001025107.3:c.2119A>T	NP_001020278.1:p.Thr707Ser
NM_001111.5:c.3004A>T MANE Select	NP_001102.3:p.Thr1002Ser
NM_001193495.2:c.2119A>T	NP_001180424.1:p.Thr707Ser
NM_001365045.1:c.3031A>T	NP_001351974.1:p.Thr1011Ser
NM_001365046.1:c.2119A>T	NP_001351975.1:p.Thr707Ser
NM_001365047.1:c.2119A>T	NP_001351976.1:p.Thr707Ser
NM_001365048.1:c.2119A>T	NP_001351977.1:p.Thr707Ser
NM_001365049.1:c.2041A>T	NP_001351978.1:p.Thr681Ser
NM_015840.4:c.2926A>T	NP_056655.3:p.Thr976Ser
NM_015841.4:c.2869A>T	NP_056656.3:p.Thr957Ser
XM_006711113.2:c.2119A>T	XP_006711176.1:p.Thr707Ser
XM_011509061.2:c.2041A>T	XP_011507363.2:p.Thr681Ser
XM_024449674.1:c.3133A>T	XP_024305442.1:p.Thr1045Ser