Canonical Allele Identifier: CA421231126

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557294G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584818G>C , CM000663.2:g.154584818G>C	GRCh38
NC_000001.10:g.154557294G>C , CM000663.1:g.154557294G>C	GRCh37
NC_000001.9:g.152823918G>C	NCBI36
NG_011844.1:g.48144C>G
NG_011844.2:g.51743C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3563C>G	ENSP00000497790.2:n.3563C>G
ENST00000649724.2:c.3699C>G	ENSP00000497932.2:p.Leu1233=
ENST00000680270.2:c.3552C>G	ENSP00000505532.2:p.Leu1184=
ENST00000681056.2:c.3321C>G	ENSP00000506234.2:p.Leu1107=
ENST00000368471.8:c.2784C>G	ENSP00000357456.3:p.Leu928=
ENST00000368474.9:c.3669C>G MANE Select	ENSP00000357459.4:p.Leu1223=
ENST00000492630.2:n.2462C>G
ENST00000529168.2:c.3591C>G	ENSP00000431794.2:p.Leu1197=
ENST00000647682.2:n.3654C>G
ENST00000648231.2:c.2784C>G	ENSP00000497555.1:p.Leu928=
ENST00000648311.1:c.2784C>G	ENSP00000498137.1:p.Leu928=
ENST00000648714.2:c.*1144C>G	ENSP00000497434.2:n.*1144C>G
ENST00000649021.1:n.4405C>G
ENST00000649022.2:c.2784C>G	ENSP00000496896.2:p.Leu928=
ENST00000649042.1:c.2784C>G	ENSP00000497790.1:p.Leu928=
ENST00000649408.2:c.*835C>G	ENSP00000497386.2:n.*835C>G
ENST00000649724.1:c.2784C>G	ENSP00000497932.1:p.Leu928=
ENST00000649749.1:c.2784C>G	ENSP00000497210.1:p.Leu928=
ENST00000679375.1:c.*1901C>G	ENSP00000505887.1:n.*1901C>G
ENST00000679465.1:n.4530C>G
ENST00000679805.1:n.4405C>G
ENST00000679899.1:c.2727C>G	ENSP00000505996.1:p.Leu909=
ENST00000680270.1:c.2784C>G	ENSP00000505532.1:p.Leu928=
ENST00000680305.1:c.3486C>G	ENSP00000506312.1:p.Leu1162=
ENST00000681056.1:c.2784C>G	ENSP00000506234.1:p.Leu928=
ENST00000681235.1:c.*3191C>G	ENSP00000506606.1:n.*3191C>G
ENST00000681429.1:n.3337C>G
ENST00000681683.1:c.2784C>G	ENSP00000506666.1:p.Leu928=
ENST00000681786.1:n.4530C>G
ENST00000681901.1:c.*3269C>G	ENSP00000504883.1:n.*3269C>G
ENST00000368471.7:c.2784C>G	ENSP00000357456.3:p.Leu928=
ENST00000368474.8:c.3669C>G	ENSP00000357459.4:p.Leu1223=
ENST00000492630.1:n.428C>G
ENST00000529168.1:c.3576C>G	ENSP00000431794.1:p.Leu1192=
NM_001025107.2:c.2784C>G	NP_001020278.1:p.Leu928=
NM_001111.4:c.3669C>G	NP_001102.2:p.Leu1223=
NM_001193495.1:c.2784C>G	NP_001180424.1:p.Leu928=
NM_015840.3:c.3591C>G	NP_056655.2:p.Leu1197=
NM_015841.3:c.3534C>G	NP_056656.2:p.Leu1178=
XM_006711109.1:c.3699C>G	XP_006711172.1:p.Leu1233=
XM_006711111.2:c.2784C>G	XP_006711174.1:p.Leu928=
XM_006711112.1:c.2784C>G	XP_006711175.1:p.Leu928=
XM_006711113.1:c.2784C>G	XP_006711176.1:p.Leu928=
XM_011509060.1:c.3798C>G	XP_011507362.1:p.Leu1266=
XM_011509061.1:c.3720C>G	XP_011507363.1:p.Leu1240=
XM_011509062.1:c.3687C>G	XP_011507364.1:p.Leu1229=
NM_001025107.3:c.2784C>G	NP_001020278.1:p.Leu928=
NM_001111.5:c.3669C>G MANE Select	NP_001102.3:p.Leu1223=
NM_001193495.2:c.2784C>G	NP_001180424.1:p.Leu928=
NM_001365045.1:c.3696C>G	NP_001351974.1:p.Leu1232=
NM_001365046.1:c.2784C>G	NP_001351975.1:p.Leu928=
NM_001365047.1:c.2784C>G	NP_001351976.1:p.Leu928=
NM_001365048.1:c.2784C>G	NP_001351977.1:p.Leu928=
NM_001365049.1:c.2706C>G	NP_001351978.1:p.Leu902=
NM_015840.4:c.3591C>G	NP_056655.3:p.Leu1197=
NM_015841.4:c.3534C>G	NP_056656.3:p.Leu1178=
XM_006711113.2:c.2784C>G	XP_006711176.1:p.Leu928=
XM_011509061.2:c.2706C>G	XP_011507363.2:p.Leu902=
XM_024449674.1:c.3798C>G	XP_024305442.1:p.Leu1266=