Canonical Allele Identifier: CA421231115

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557291G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584815G>A , CM000663.2:g.154584815G>A	GRCh38
NC_000001.10:g.154557291G>A , CM000663.1:g.154557291G>A	GRCh37
NC_000001.9:g.152823915G>A	NCBI36
NG_011844.1:g.48147C>T
NG_011844.2:g.51746C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3566C>T	ENSP00000497790.2:n.3566C>T
ENST00000649724.2:c.3702C>T	ENSP00000497932.2:p.Cys1234=
ENST00000680270.2:c.3555C>T	ENSP00000505532.2:p.Cys1185=
ENST00000681056.2:c.3324C>T	ENSP00000506234.2:p.Cys1108=
ENST00000368471.8:c.2787C>T	ENSP00000357456.3:p.Cys929=
ENST00000368474.9:c.3672C>T MANE Select	ENSP00000357459.4:p.Cys1224=
ENST00000492630.2:n.2465C>T
ENST00000529168.2:c.3594C>T	ENSP00000431794.2:p.Cys1198=
ENST00000647682.2:n.3657C>T
ENST00000648231.2:c.2787C>T	ENSP00000497555.1:p.Cys929=
ENST00000648311.1:c.2787C>T	ENSP00000498137.1:p.Cys929=
ENST00000648714.2:c.*1147C>T	ENSP00000497434.2:n.*1147C>T
ENST00000649021.1:n.4408C>T
ENST00000649022.2:c.2787C>T	ENSP00000496896.2:p.Cys929=
ENST00000649042.1:c.2787C>T	ENSP00000497790.1:p.Cys929=
ENST00000649408.2:c.*838C>T	ENSP00000497386.2:n.*838C>T
ENST00000649724.1:c.2787C>T	ENSP00000497932.1:p.Cys929=
ENST00000649749.1:c.2787C>T	ENSP00000497210.1:p.Cys929=
ENST00000679375.1:c.*1904C>T	ENSP00000505887.1:n.*1904C>T
ENST00000679465.1:n.4533C>T
ENST00000679805.1:n.4408C>T
ENST00000679899.1:c.2730C>T	ENSP00000505996.1:p.Cys910=
ENST00000680270.1:c.2787C>T	ENSP00000505532.1:p.Cys929=
ENST00000680305.1:c.3489C>T	ENSP00000506312.1:p.Cys1163=
ENST00000681056.1:c.2787C>T	ENSP00000506234.1:p.Cys929=
ENST00000681235.1:c.*3194C>T	ENSP00000506606.1:n.*3194C>T
ENST00000681429.1:n.3340C>T
ENST00000681683.1:c.2787C>T	ENSP00000506666.1:p.Cys929=
ENST00000681786.1:n.4533C>T
ENST00000681901.1:c.*3272C>T	ENSP00000504883.1:n.*3272C>T
ENST00000368471.7:c.2787C>T	ENSP00000357456.3:p.Cys929=
ENST00000368474.8:c.3672C>T	ENSP00000357459.4:p.Cys1224=
ENST00000492630.1:n.431C>T
ENST00000529168.1:c.3579C>T	ENSP00000431794.1:p.Cys1193=
NM_001025107.2:c.2787C>T	NP_001020278.1:p.Cys929=
NM_001111.4:c.3672C>T	NP_001102.2:p.Cys1224=
NM_001193495.1:c.2787C>T	NP_001180424.1:p.Cys929=
NM_015840.3:c.3594C>T	NP_056655.2:p.Cys1198=
NM_015841.3:c.3537C>T	NP_056656.2:p.Cys1179=
XM_006711109.1:c.3702C>T	XP_006711172.1:p.Cys1234=
XM_006711111.2:c.2787C>T	XP_006711174.1:p.Cys929=
XM_006711112.1:c.2787C>T	XP_006711175.1:p.Cys929=
XM_006711113.1:c.2787C>T	XP_006711176.1:p.Cys929=
XM_011509060.1:c.3801C>T	XP_011507362.1:p.Cys1267=
XM_011509061.1:c.3723C>T	XP_011507363.1:p.Cys1241=
XM_011509062.1:c.3690C>T	XP_011507364.1:p.Cys1230=
NM_001025107.3:c.2787C>T	NP_001020278.1:p.Cys929=
NM_001111.5:c.3672C>T MANE Select	NP_001102.3:p.Cys1224=
NM_001193495.2:c.2787C>T	NP_001180424.1:p.Cys929=
NM_001365045.1:c.3699C>T	NP_001351974.1:p.Cys1233=
NM_001365046.1:c.2787C>T	NP_001351975.1:p.Cys929=
NM_001365047.1:c.2787C>T	NP_001351976.1:p.Cys929=
NM_001365048.1:c.2787C>T	NP_001351977.1:p.Cys929=
NM_001365049.1:c.2709C>T	NP_001351978.1:p.Cys903=
NM_015840.4:c.3594C>T	NP_056655.3:p.Cys1198=
NM_015841.4:c.3537C>T	NP_056656.3:p.Cys1179=
XM_006711113.2:c.2787C>T	XP_006711176.1:p.Cys929=
XM_011509061.2:c.2709C>T	XP_011507363.2:p.Cys903=
XM_024449674.1:c.3801C>T	XP_024305442.1:p.Cys1267=