Canonical Allele Identifier: CA421231449

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557390G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584914G>A , CM000663.2:g.154584914G>A	GRCh38
NC_000001.10:g.154557390G>A , CM000663.1:g.154557390G>A	GRCh37
NC_000001.9:g.152824014G>A	NCBI36
NG_011844.1:g.48048C>T
NG_011844.2:g.51647C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3467C>T	ENSP00000497790.2:n.3467C>T
ENST00000649724.2:c.3603C>T	ENSP00000497932.2:p.Asp1201=
ENST00000680270.2:c.3456C>T	ENSP00000505532.2:p.Asp1152=
ENST00000681056.2:c.3225C>T	ENSP00000506234.2:p.Asp1075=
ENST00000368471.8:c.2688C>T	ENSP00000357456.3:p.Asp896=
ENST00000368474.9:c.3573C>T MANE Select	ENSP00000357459.4:p.Asp1191=
ENST00000492630.2:n.2366C>T
ENST00000529168.2:c.3495C>T	ENSP00000431794.2:p.Asp1165=
ENST00000647682.2:n.3558C>T
ENST00000648231.2:c.2688C>T	ENSP00000497555.1:p.Asp896=
ENST00000648311.1:c.2688C>T	ENSP00000498137.1:p.Asp896=
ENST00000648714.2:c.*1048C>T	ENSP00000497434.2:n.*1048C>T
ENST00000649021.1:n.4309C>T
ENST00000649022.2:c.2688C>T	ENSP00000496896.2:p.Asp896=
ENST00000649042.1:c.2688C>T	ENSP00000497790.1:p.Asp896=
ENST00000649408.2:c.*739C>T	ENSP00000497386.2:n.*739C>T
ENST00000649724.1:c.2688C>T	ENSP00000497932.1:p.Asp896=
ENST00000649749.1:c.2688C>T	ENSP00000497210.1:p.Asp896=
ENST00000679375.1:c.*1805C>T	ENSP00000505887.1:n.*1805C>T
ENST00000679465.1:n.4434C>T
ENST00000679805.1:n.4309C>T
ENST00000679899.1:c.2631C>T	ENSP00000505996.1:p.Asp877=
ENST00000680270.1:c.2688C>T	ENSP00000505532.1:p.Asp896=
ENST00000680305.1:c.3390C>T	ENSP00000506312.1:p.Asp1130=
ENST00000681056.1:c.2688C>T	ENSP00000506234.1:p.Asp896=
ENST00000681235.1:c.*3095C>T	ENSP00000506606.1:n.*3095C>T
ENST00000681429.1:n.3241C>T
ENST00000681683.1:c.2688C>T	ENSP00000506666.1:p.Asp896=
ENST00000681786.1:n.4434C>T
ENST00000681901.1:c.*3173C>T	ENSP00000504883.1:n.*3173C>T
ENST00000368471.7:c.2688C>T	ENSP00000357456.3:p.Asp896=
ENST00000368474.8:c.3573C>T	ENSP00000357459.4:p.Asp1191=
ENST00000492630.1:n.332C>T
ENST00000529168.1:c.3480C>T	ENSP00000431794.1:p.Asp1160=
NM_001025107.2:c.2688C>T	NP_001020278.1:p.Asp896=
NM_001111.4:c.3573C>T	NP_001102.2:p.Asp1191=
NM_001193495.1:c.2688C>T	NP_001180424.1:p.Asp896=
NM_015840.3:c.3495C>T	NP_056655.2:p.Asp1165=
NM_015841.3:c.3438C>T	NP_056656.2:p.Asp1146=
XM_006711109.1:c.3603C>T	XP_006711172.1:p.Asp1201=
XM_006711111.2:c.2688C>T	XP_006711174.1:p.Asp896=
XM_006711112.1:c.2688C>T	XP_006711175.1:p.Asp896=
XM_006711113.1:c.2688C>T	XP_006711176.1:p.Asp896=
XM_011509060.1:c.3702C>T	XP_011507362.1:p.Asp1234=
XM_011509061.1:c.3624C>T	XP_011507363.1:p.Asp1208=
XM_011509062.1:c.3591C>T	XP_011507364.1:p.Asp1197=
NM_001025107.3:c.2688C>T	NP_001020278.1:p.Asp896=
NM_001111.5:c.3573C>T MANE Select	NP_001102.3:p.Asp1191=
NM_001193495.2:c.2688C>T	NP_001180424.1:p.Asp896=
NM_001365045.1:c.3600C>T	NP_001351974.1:p.Asp1200=
NM_001365046.1:c.2688C>T	NP_001351975.1:p.Asp896=
NM_001365047.1:c.2688C>T	NP_001351976.1:p.Asp896=
NM_001365048.1:c.2688C>T	NP_001351977.1:p.Asp896=
NM_001365049.1:c.2610C>T	NP_001351978.1:p.Asp870=
NM_015840.4:c.3495C>T	NP_056655.3:p.Asp1165=
NM_015841.4:c.3438C>T	NP_056656.3:p.Asp1146=
XM_006711113.2:c.2688C>T	XP_006711176.1:p.Asp896=
XM_011509061.2:c.2610C>T	XP_011507363.2:p.Asp870=
XM_024449674.1:c.3702C>T	XP_024305442.1:p.Asp1234=