Canonical Allele Identifier: CA342635979

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154560629T>G (hg19) ; chr1:g.154588153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588153T>G , CM000663.2:g.154588153T>G	GRCh38
NC_000001.10:g.154560629T>G , CM000663.1:g.154560629T>G	GRCh37
NC_000001.9:g.152827253T>G	NCBI36
NG_011844.1:g.44809A>C
NG_011844.2:g.48408A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.2885A>C	ENSP00000497790.2:n.2885A>C
ENST00000649724.2:c.3021A>C	ENSP00000497932.2:p.Gln1007His
ENST00000680270.2:c.2874A>C	ENSP00000505532.2:p.Gln958His
ENST00000681056.2:c.2643A>C	ENSP00000506234.2:p.Gln881His
ENST00000368471.8:c.2106A>C	ENSP00000357456.3:p.Gln702His
ENST00000368474.9:c.2991A>C MANE Select	ENSP00000357459.4:p.Gln997His
ENST00000529168.2:c.2913A>C	ENSP00000431794.2:p.Gln971His
ENST00000647682.2:n.2976A>C
ENST00000648231.2:c.2106A>C	ENSP00000497555.1:p.Gln702His
ENST00000648311.1:c.2106A>C	ENSP00000498137.1:p.Gln702His
ENST00000648714.2:c.*466A>C	ENSP00000497434.2:n.*466A>C
ENST00000649021.1:n.3319A>C
ENST00000649022.2:c.2106A>C	ENSP00000496896.2:p.Gln702His
ENST00000649042.1:c.2106A>C	ENSP00000497790.1:p.Gln702His
ENST00000649408.2:c.2991A>C	ENSP00000497386.2:p.Gln997His
ENST00000649724.1:c.2106A>C	ENSP00000497932.1:p.Gln702His
ENST00000649749.1:c.2106A>C	ENSP00000497210.1:p.Gln702His
ENST00000679375.1:c.*1223A>C	ENSP00000505887.1:n.*1223A>C
ENST00000679465.1:n.3444A>C
ENST00000679805.1:n.3319A>C
ENST00000679899.1:c.2049A>C	ENSP00000505996.1:p.Gln683His
ENST00000680270.1:c.2106A>C	ENSP00000505532.1:p.Gln702His
ENST00000680305.1:c.2991A>C	ENSP00000506312.1:p.Gln997His
ENST00000681056.1:c.2106A>C	ENSP00000506234.1:p.Gln702His
ENST00000681235.1:c.*2513A>C	ENSP00000506606.1:n.*2513A>C
ENST00000681429.1:n.2251A>C
ENST00000681683.1:c.2106A>C	ENSP00000506666.1:p.Gln702His
ENST00000681786.1:n.3444A>C
ENST00000681901.1:c.*2591A>C	ENSP00000504883.1:n.*2591A>C
ENST00000368471.7:c.2106A>C	ENSP00000357456.3:p.Gln702His
ENST00000368474.8:c.2991A>C	ENSP00000357459.4:p.Gln997His
ENST00000529168.1:c.2898A>C	ENSP00000431794.1:p.Gln966His
ENST00000530954.1:n.128A>C
ENST00000534279.1:n.450A>C
NM_001025107.2:c.2106A>C	NP_001020278.1:p.Gln702His
NM_001111.4:c.2991A>C	NP_001102.2:p.Gln997His
NM_001193495.1:c.2106A>C	NP_001180424.1:p.Gln702His
NM_015840.3:c.2913A>C	NP_056655.2:p.Gln971His
NM_015841.3:c.2856A>C	NP_056656.2:p.Gln952His
XM_006711109.1:c.3021A>C	XP_006711172.1:p.Gln1007His
XM_006711111.2:c.2106A>C	XP_006711174.1:p.Gln702His
XM_006711112.1:c.2106A>C	XP_006711175.1:p.Gln702His
XM_006711113.1:c.2106A>C	XP_006711176.1:p.Gln702His
XM_011509060.1:c.3120A>C	XP_011507362.1:p.Gln1040His
XM_011509061.1:c.3042A>C	XP_011507363.1:p.Gln1014His
XM_011509062.1:c.3009A>C	XP_011507364.1:p.Gln1003His
NM_001025107.3:c.2106A>C	NP_001020278.1:p.Gln702His
NM_001111.5:c.2991A>C MANE Select	NP_001102.3:p.Gln997His
NM_001193495.2:c.2106A>C	NP_001180424.1:p.Gln702His
NM_001365045.1:c.3018A>C	NP_001351974.1:p.Gln1006His
NM_001365046.1:c.2106A>C	NP_001351975.1:p.Gln702His
NM_001365047.1:c.2106A>C	NP_001351976.1:p.Gln702His
NM_001365048.1:c.2106A>C	NP_001351977.1:p.Gln702His
NM_001365049.1:c.2028A>C	NP_001351978.1:p.Gln676His
NM_015840.4:c.2913A>C	NP_056655.3:p.Gln971His
NM_015841.4:c.2856A>C	NP_056656.3:p.Gln952His
XM_006711113.2:c.2106A>C	XP_006711176.1:p.Gln702His
XM_011509061.2:c.2028A>C	XP_011507363.2:p.Gln676His
XM_024449674.1:c.3120A>C	XP_024305442.1:p.Gln1040His