Canonical Allele Identifier: CA1130920

Gene: ADAR

Linked Data

• dbSNP Id: rs370464259
• ExAC: 1:154557396 G / A
• gnomAD v2: 1-154557396-G-A
• gnomAD v3: 1-154584920-G-A
• gnomAD v4: 1-154584920-G-A
• MyVariant Identifiers: chr1:g.154557396G>A (hg19) ; chr1:g.154584920G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584920G>A , CM000663.2:g.154584920G>A	GRCh38
NC_000001.10:g.154557396G>A , CM000663.1:g.154557396G>A	GRCh37
NC_000001.9:g.152824020G>A	NCBI36
NG_011844.1:g.48042C>T
NG_011844.2:g.51641C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3461C>T	ENSP00000497790.2:n.3461C>T
ENST00000649724.2:c.3597C>T	ENSP00000497932.2:p.Ala1199=
ENST00000680270.2:c.3450C>T	ENSP00000505532.2:p.Ala1150=
ENST00000681056.2:c.3219C>T	ENSP00000506234.2:p.Ala1073=
ENST00000368471.8:c.2682C>T	ENSP00000357456.3:p.Ala894=
ENST00000368474.9:c.3567C>T MANE Select	ENSP00000357459.4:p.Ala1189=
ENST00000492630.2:n.2360C>T
ENST00000529168.2:c.3489C>T	ENSP00000431794.2:p.Ala1163=
ENST00000647682.2:n.3552C>T
ENST00000648231.2:c.2682C>T	ENSP00000497555.1:p.Ala894=
ENST00000648311.1:c.2682C>T	ENSP00000498137.1:p.Ala894=
ENST00000648714.2:c.*1042C>T	ENSP00000497434.2:n.*1042C>T
ENST00000649021.1:n.4303C>T
ENST00000649022.2:c.2682C>T	ENSP00000496896.2:p.Ala894=
ENST00000649042.1:c.2682C>T	ENSP00000497790.1:p.Ala894=
ENST00000649408.2:c.*733C>T	ENSP00000497386.2:n.*733C>T
ENST00000649724.1:c.2682C>T	ENSP00000497932.1:p.Ala894=
ENST00000649749.1:c.2682C>T	ENSP00000497210.1:p.Ala894=
ENST00000679375.1:c.*1799C>T	ENSP00000505887.1:n.*1799C>T
ENST00000679465.1:n.4428C>T
ENST00000679805.1:n.4303C>T
ENST00000679899.1:c.2625C>T	ENSP00000505996.1:p.Ala875=
ENST00000680270.1:c.2682C>T	ENSP00000505532.1:p.Ala894=
ENST00000680305.1:c.3384C>T	ENSP00000506312.1:p.Ala1128=
ENST00000681056.1:c.2682C>T	ENSP00000506234.1:p.Ala894=
ENST00000681235.1:c.*3089C>T	ENSP00000506606.1:n.*3089C>T
ENST00000681429.1:n.3235C>T
ENST00000681683.1:c.2682C>T	ENSP00000506666.1:p.Ala894=
ENST00000681786.1:n.4428C>T
ENST00000681901.1:c.*3167C>T	ENSP00000504883.1:n.*3167C>T
ENST00000368471.7:c.2682C>T	ENSP00000357456.3:p.Ala894=
ENST00000368474.8:c.3567C>T	ENSP00000357459.4:p.Ala1189=
ENST00000492630.1:n.326C>T
ENST00000529168.1:c.3474C>T	ENSP00000431794.1:p.Ala1158=
NM_001025107.2:c.2682C>T	NP_001020278.1:p.Ala894=
NM_001111.4:c.3567C>T	NP_001102.2:p.Ala1189=
NM_001193495.1:c.2682C>T	NP_001180424.1:p.Ala894=
NM_015840.3:c.3489C>T	NP_056655.2:p.Ala1163=
NM_015841.3:c.3432C>T	NP_056656.2:p.Ala1144=
XM_006711109.1:c.3597C>T	XP_006711172.1:p.Ala1199=
XM_006711111.2:c.2682C>T	XP_006711174.1:p.Ala894=
XM_006711112.1:c.2682C>T	XP_006711175.1:p.Ala894=
XM_006711113.1:c.2682C>T	XP_006711176.1:p.Ala894=
XM_011509060.1:c.3696C>T	XP_011507362.1:p.Ala1232=
XM_011509061.1:c.3618C>T	XP_011507363.1:p.Ala1206=
XM_011509062.1:c.3585C>T	XP_011507364.1:p.Ala1195=
NM_001025107.3:c.2682C>T	NP_001020278.1:p.Ala894=
NM_001111.5:c.3567C>T MANE Select	NP_001102.3:p.Ala1189=
NM_001193495.2:c.2682C>T	NP_001180424.1:p.Ala894=
NM_001365045.1:c.3594C>T	NP_001351974.1:p.Ala1198=
NM_001365046.1:c.2682C>T	NP_001351975.1:p.Ala894=
NM_001365047.1:c.2682C>T	NP_001351976.1:p.Ala894=
NM_001365048.1:c.2682C>T	NP_001351977.1:p.Ala894=
NM_001365049.1:c.2604C>T	NP_001351978.1:p.Ala868=
NM_015840.4:c.3489C>T	NP_056655.3:p.Ala1163=
NM_015841.4:c.3432C>T	NP_056656.3:p.Ala1144=
XM_006711113.2:c.2682C>T	XP_006711176.1:p.Ala894=
XM_011509061.2:c.2604C>T	XP_011507363.2:p.Ala868=
XM_024449674.1:c.3696C>T	XP_024305442.1:p.Ala1232=