Canonical Allele Identifier: CA342634683

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557398C>T (hg19) ; chr1:g.154584922C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584922C>T , CM000663.2:g.154584922C>T	GRCh38
NC_000001.10:g.154557398C>T , CM000663.1:g.154557398C>T	GRCh37
NC_000001.9:g.152824022C>T	NCBI36
NG_011844.1:g.48040G>A
NG_011844.2:g.51639G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3459G>A	ENSP00000497790.2:n.3459G>A
ENST00000649724.2:c.3595G>A	ENSP00000497932.2:p.Ala1199Thr
ENST00000680270.2:c.3448G>A	ENSP00000505532.2:p.Ala1150Thr
ENST00000681056.2:c.3217G>A	ENSP00000506234.2:p.Ala1073Thr
ENST00000368471.8:c.2680G>A	ENSP00000357456.3:p.Ala894Thr
ENST00000368474.9:c.3565G>A MANE Select	ENSP00000357459.4:p.Ala1189Thr
ENST00000492630.2:n.2358G>A
ENST00000529168.2:c.3487G>A	ENSP00000431794.2:p.Ala1163Thr
ENST00000647682.2:n.3550G>A
ENST00000648231.2:c.2680G>A	ENSP00000497555.1:p.Ala894Thr
ENST00000648311.1:c.2680G>A	ENSP00000498137.1:p.Ala894Thr
ENST00000648714.2:c.*1040G>A	ENSP00000497434.2:n.*1040G>A
ENST00000649021.1:n.4301G>A
ENST00000649022.2:c.2680G>A	ENSP00000496896.2:p.Ala894Thr
ENST00000649042.1:c.2680G>A	ENSP00000497790.1:p.Ala894Thr
ENST00000649408.2:c.*731G>A	ENSP00000497386.2:n.*731G>A
ENST00000649724.1:c.2680G>A	ENSP00000497932.1:p.Ala894Thr
ENST00000649749.1:c.2680G>A	ENSP00000497210.1:p.Ala894Thr
ENST00000679375.1:c.*1797G>A	ENSP00000505887.1:n.*1797G>A
ENST00000679465.1:n.4426G>A
ENST00000679805.1:n.4301G>A
ENST00000679899.1:c.2623G>A	ENSP00000505996.1:p.Ala875Thr
ENST00000680270.1:c.2680G>A	ENSP00000505532.1:p.Ala894Thr
ENST00000680305.1:c.3382G>A	ENSP00000506312.1:p.Ala1128Thr
ENST00000681056.1:c.2680G>A	ENSP00000506234.1:p.Ala894Thr
ENST00000681235.1:c.*3087G>A	ENSP00000506606.1:n.*3087G>A
ENST00000681429.1:n.3233G>A
ENST00000681683.1:c.2680G>A	ENSP00000506666.1:p.Ala894Thr
ENST00000681786.1:n.4426G>A
ENST00000681901.1:c.*3165G>A	ENSP00000504883.1:n.*3165G>A
ENST00000368471.7:c.2680G>A	ENSP00000357456.3:p.Ala894Thr
ENST00000368474.8:c.3565G>A	ENSP00000357459.4:p.Ala1189Thr
ENST00000492630.1:n.324G>A
ENST00000529168.1:c.3472G>A	ENSP00000431794.1:p.Ala1158Thr
NM_001025107.2:c.2680G>A	NP_001020278.1:p.Ala894Thr
NM_001111.4:c.3565G>A	NP_001102.2:p.Ala1189Thr
NM_001193495.1:c.2680G>A	NP_001180424.1:p.Ala894Thr
NM_015840.3:c.3487G>A	NP_056655.2:p.Ala1163Thr
NM_015841.3:c.3430G>A	NP_056656.2:p.Ala1144Thr
XM_006711109.1:c.3595G>A	XP_006711172.1:p.Ala1199Thr
XM_006711111.2:c.2680G>A	XP_006711174.1:p.Ala894Thr
XM_006711112.1:c.2680G>A	XP_006711175.1:p.Ala894Thr
XM_006711113.1:c.2680G>A	XP_006711176.1:p.Ala894Thr
XM_011509060.1:c.3694G>A	XP_011507362.1:p.Ala1232Thr
XM_011509061.1:c.3616G>A	XP_011507363.1:p.Ala1206Thr
XM_011509062.1:c.3583G>A	XP_011507364.1:p.Ala1195Thr
NM_001025107.3:c.2680G>A	NP_001020278.1:p.Ala894Thr
NM_001111.5:c.3565G>A MANE Select	NP_001102.3:p.Ala1189Thr
NM_001193495.2:c.2680G>A	NP_001180424.1:p.Ala894Thr
NM_001365045.1:c.3592G>A	NP_001351974.1:p.Ala1198Thr
NM_001365046.1:c.2680G>A	NP_001351975.1:p.Ala894Thr
NM_001365047.1:c.2680G>A	NP_001351976.1:p.Ala894Thr
NM_001365048.1:c.2680G>A	NP_001351977.1:p.Ala894Thr
NM_001365049.1:c.2602G>A	NP_001351978.1:p.Ala868Thr
NM_015840.4:c.3487G>A	NP_056655.3:p.Ala1163Thr
NM_015841.4:c.3430G>A	NP_056656.3:p.Ala1144Thr
XM_006711113.2:c.2680G>A	XP_006711176.1:p.Ala894Thr
XM_011509061.2:c.2602G>A	XP_011507363.2:p.Ala868Thr
XM_024449674.1:c.3694G>A	XP_024305442.1:p.Ala1232Thr