Canonical Allele Identifier: CA342634681

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557397G>T (hg19) ; chr1:g.154584921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584921G>T , CM000663.2:g.154584921G>T	GRCh38
NC_000001.10:g.154557397G>T , CM000663.1:g.154557397G>T	GRCh37
NC_000001.9:g.152824021G>T	NCBI36
NG_011844.1:g.48041C>A
NG_011844.2:g.51640C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3460C>A	ENSP00000497790.2:n.3460C>A
ENST00000649724.2:c.3596C>A	ENSP00000497932.2:p.Ala1199Asp
ENST00000680270.2:c.3449C>A	ENSP00000505532.2:p.Ala1150Asp
ENST00000681056.2:c.3218C>A	ENSP00000506234.2:p.Ala1073Asp
ENST00000368471.8:c.2681C>A	ENSP00000357456.3:p.Ala894Asp
ENST00000368474.9:c.3566C>A MANE Select	ENSP00000357459.4:p.Ala1189Asp
ENST00000492630.2:n.2359C>A
ENST00000529168.2:c.3488C>A	ENSP00000431794.2:p.Ala1163Asp
ENST00000647682.2:n.3551C>A
ENST00000648231.2:c.2681C>A	ENSP00000497555.1:p.Ala894Asp
ENST00000648311.1:c.2681C>A	ENSP00000498137.1:p.Ala894Asp
ENST00000648714.2:c.*1041C>A	ENSP00000497434.2:n.*1041C>A
ENST00000649021.1:n.4302C>A
ENST00000649022.2:c.2681C>A	ENSP00000496896.2:p.Ala894Asp
ENST00000649042.1:c.2681C>A	ENSP00000497790.1:p.Ala894Asp
ENST00000649408.2:c.*732C>A	ENSP00000497386.2:n.*732C>A
ENST00000649724.1:c.2681C>A	ENSP00000497932.1:p.Ala894Asp
ENST00000649749.1:c.2681C>A	ENSP00000497210.1:p.Ala894Asp
ENST00000679375.1:c.*1798C>A	ENSP00000505887.1:n.*1798C>A
ENST00000679465.1:n.4427C>A
ENST00000679805.1:n.4302C>A
ENST00000679899.1:c.2624C>A	ENSP00000505996.1:p.Ala875Asp
ENST00000680270.1:c.2681C>A	ENSP00000505532.1:p.Ala894Asp
ENST00000680305.1:c.3383C>A	ENSP00000506312.1:p.Ala1128Asp
ENST00000681056.1:c.2681C>A	ENSP00000506234.1:p.Ala894Asp
ENST00000681235.1:c.*3088C>A	ENSP00000506606.1:n.*3088C>A
ENST00000681429.1:n.3234C>A
ENST00000681683.1:c.2681C>A	ENSP00000506666.1:p.Ala894Asp
ENST00000681786.1:n.4427C>A
ENST00000681901.1:c.*3166C>A	ENSP00000504883.1:n.*3166C>A
ENST00000368471.7:c.2681C>A	ENSP00000357456.3:p.Ala894Asp
ENST00000368474.8:c.3566C>A	ENSP00000357459.4:p.Ala1189Asp
ENST00000492630.1:n.325C>A
ENST00000529168.1:c.3473C>A	ENSP00000431794.1:p.Ala1158Asp
NM_001025107.2:c.2681C>A	NP_001020278.1:p.Ala894Asp
NM_001111.4:c.3566C>A	NP_001102.2:p.Ala1189Asp
NM_001193495.1:c.2681C>A	NP_001180424.1:p.Ala894Asp
NM_015840.3:c.3488C>A	NP_056655.2:p.Ala1163Asp
NM_015841.3:c.3431C>A	NP_056656.2:p.Ala1144Asp
XM_006711109.1:c.3596C>A	XP_006711172.1:p.Ala1199Asp
XM_006711111.2:c.2681C>A	XP_006711174.1:p.Ala894Asp
XM_006711112.1:c.2681C>A	XP_006711175.1:p.Ala894Asp
XM_006711113.1:c.2681C>A	XP_006711176.1:p.Ala894Asp
XM_011509060.1:c.3695C>A	XP_011507362.1:p.Ala1232Asp
XM_011509061.1:c.3617C>A	XP_011507363.1:p.Ala1206Asp
XM_011509062.1:c.3584C>A	XP_011507364.1:p.Ala1195Asp
NM_001025107.3:c.2681C>A	NP_001020278.1:p.Ala894Asp
NM_001111.5:c.3566C>A MANE Select	NP_001102.3:p.Ala1189Asp
NM_001193495.2:c.2681C>A	NP_001180424.1:p.Ala894Asp
NM_001365045.1:c.3593C>A	NP_001351974.1:p.Ala1198Asp
NM_001365046.1:c.2681C>A	NP_001351975.1:p.Ala894Asp
NM_001365047.1:c.2681C>A	NP_001351976.1:p.Ala894Asp
NM_001365048.1:c.2681C>A	NP_001351977.1:p.Ala894Asp
NM_001365049.1:c.2603C>A	NP_001351978.1:p.Ala868Asp
NM_015840.4:c.3488C>A	NP_056655.3:p.Ala1163Asp
NM_015841.4:c.3431C>A	NP_056656.3:p.Ala1144Asp
XM_006711113.2:c.2681C>A	XP_006711176.1:p.Ala894Asp
XM_011509061.2:c.2603C>A	XP_011507363.2:p.Ala868Asp
XM_024449674.1:c.3695C>A	XP_024305442.1:p.Ala1232Asp