Canonical Allele Identifier: CA342634657

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557386C>A (hg19) ; chr1:g.154584910C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584910C>A , CM000663.2:g.154584910C>A	GRCh38
NC_000001.10:g.154557386C>A , CM000663.1:g.154557386C>A	GRCh37
NC_000001.9:g.152824010C>A	NCBI36
NG_011844.1:g.48052G>T
NG_011844.2:g.51651G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3471G>T	ENSP00000497790.2:n.3471G>T
ENST00000649724.2:c.3607G>T	ENSP00000497932.2:p.Glu1203Ter
ENST00000680270.2:c.3460G>T	ENSP00000505532.2:p.Glu1154Ter
ENST00000681056.2:c.3229G>T	ENSP00000506234.2:p.Glu1077Ter
ENST00000368471.8:c.2692G>T	ENSP00000357456.3:p.Glu898Ter
ENST00000368474.9:c.3577G>T MANE Select	ENSP00000357459.4:p.Glu1193Ter
ENST00000492630.2:n.2370G>T
ENST00000529168.2:c.3499G>T	ENSP00000431794.2:p.Glu1167Ter
ENST00000647682.2:n.3562G>T
ENST00000648231.2:c.2692G>T	ENSP00000497555.1:p.Glu898Ter
ENST00000648311.1:c.2692G>T	ENSP00000498137.1:p.Glu898Ter
ENST00000648714.2:c.*1052G>T	ENSP00000497434.2:n.*1052G>T
ENST00000649021.1:n.4313G>T
ENST00000649022.2:c.2692G>T	ENSP00000496896.2:p.Glu898Ter
ENST00000649042.1:c.2692G>T	ENSP00000497790.1:p.Glu898Ter
ENST00000649408.2:c.*743G>T	ENSP00000497386.2:n.*743G>T
ENST00000649724.1:c.2692G>T	ENSP00000497932.1:p.Glu898Ter
ENST00000649749.1:c.2692G>T	ENSP00000497210.1:p.Glu898Ter
ENST00000679375.1:c.*1809G>T	ENSP00000505887.1:n.*1809G>T
ENST00000679465.1:n.4438G>T
ENST00000679805.1:n.4313G>T
ENST00000679899.1:c.2635G>T	ENSP00000505996.1:p.Glu879Ter
ENST00000680270.1:c.2692G>T	ENSP00000505532.1:p.Glu898Ter
ENST00000680305.1:c.3394G>T	ENSP00000506312.1:p.Glu1132Ter
ENST00000681056.1:c.2692G>T	ENSP00000506234.1:p.Glu898Ter
ENST00000681235.1:c.*3099G>T	ENSP00000506606.1:n.*3099G>T
ENST00000681429.1:n.3245G>T
ENST00000681683.1:c.2692G>T	ENSP00000506666.1:p.Glu898Ter
ENST00000681786.1:n.4438G>T
ENST00000681901.1:c.*3177G>T	ENSP00000504883.1:n.*3177G>T
ENST00000368471.7:c.2692G>T	ENSP00000357456.3:p.Glu898Ter
ENST00000368474.8:c.3577G>T	ENSP00000357459.4:p.Glu1193Ter
ENST00000492630.1:n.336G>T
ENST00000529168.1:c.3484G>T	ENSP00000431794.1:p.Glu1162Ter
NM_001025107.2:c.2692G>T	NP_001020278.1:p.Glu898Ter
NM_001111.4:c.3577G>T	NP_001102.2:p.Glu1193Ter
NM_001193495.1:c.2692G>T	NP_001180424.1:p.Glu898Ter
NM_015840.3:c.3499G>T	NP_056655.2:p.Glu1167Ter
NM_015841.3:c.3442G>T	NP_056656.2:p.Glu1148Ter
XM_006711109.1:c.3607G>T	XP_006711172.1:p.Glu1203Ter
XM_006711111.2:c.2692G>T	XP_006711174.1:p.Glu898Ter
XM_006711112.1:c.2692G>T	XP_006711175.1:p.Glu898Ter
XM_006711113.1:c.2692G>T	XP_006711176.1:p.Glu898Ter
XM_011509060.1:c.3706G>T	XP_011507362.1:p.Glu1236Ter
XM_011509061.1:c.3628G>T	XP_011507363.1:p.Glu1210Ter
XM_011509062.1:c.3595G>T	XP_011507364.1:p.Glu1199Ter
NM_001025107.3:c.2692G>T	NP_001020278.1:p.Glu898Ter
NM_001111.5:c.3577G>T MANE Select	NP_001102.3:p.Glu1193Ter
NM_001193495.2:c.2692G>T	NP_001180424.1:p.Glu898Ter
NM_001365045.1:c.3604G>T	NP_001351974.1:p.Glu1202Ter
NM_001365046.1:c.2692G>T	NP_001351975.1:p.Glu898Ter
NM_001365047.1:c.2692G>T	NP_001351976.1:p.Glu898Ter
NM_001365048.1:c.2692G>T	NP_001351977.1:p.Glu898Ter
NM_001365049.1:c.2614G>T	NP_001351978.1:p.Glu872Ter
NM_015840.4:c.3499G>T	NP_056655.3:p.Glu1167Ter
NM_015841.4:c.3442G>T	NP_056656.3:p.Glu1148Ter
XM_006711113.2:c.2692G>T	XP_006711176.1:p.Glu898Ter
XM_011509061.2:c.2614G>T	XP_011507363.2:p.Glu872Ter
XM_024449674.1:c.3706G>T	XP_024305442.1:p.Glu1236Ter