Canonical Allele Identifier: CA420974574

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557809G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585333G>T , CM000663.2:g.154585333G>T	GRCh38
NC_000001.10:g.154557809G>T , CM000663.1:g.154557809G>T	GRCh37
NC_000001.9:g.152824433G>T	NCBI36
NG_011844.1:g.47629C>A
NG_011844.2:g.51228C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3221C>A	ENSP00000497790.2:n.3221C>A
ENST00000649724.2:c.3357C>A	ENSP00000497932.2:p.Val1119=
ENST00000680270.2:c.3210C>A	ENSP00000505532.2:p.Val1070=
ENST00000681056.2:c.2979C>A	ENSP00000506234.2:p.Val993=
ENST00000368471.8:c.2442C>A	ENSP00000357456.3:p.Val814=
ENST00000368474.9:c.3327C>A MANE Select	ENSP00000357459.4:p.Val1109=
ENST00000492630.2:n.2120C>A
ENST00000529168.2:c.3249C>A	ENSP00000431794.2:p.Val1083=
ENST00000647682.2:n.3312C>A
ENST00000648231.2:c.2442C>A	ENSP00000497555.1:p.Val814=
ENST00000648311.1:c.2442C>A	ENSP00000498137.1:p.Val814=
ENST00000648714.2:c.*802C>A	ENSP00000497434.2:n.*802C>A
ENST00000649021.1:n.4063C>A
ENST00000649022.2:c.2442C>A	ENSP00000496896.2:p.Val814=
ENST00000649042.1:c.2442C>A	ENSP00000497790.1:p.Val814=
ENST00000649408.2:c.*493C>A	ENSP00000497386.2:n.*493C>A
ENST00000649724.1:c.2442C>A	ENSP00000497932.1:p.Val814=
ENST00000649749.1:c.2442C>A	ENSP00000497210.1:p.Val814=
ENST00000679375.1:c.*1559C>A	ENSP00000505887.1:n.*1559C>A
ENST00000679465.1:n.4188C>A
ENST00000679805.1:n.4063C>A
ENST00000679899.1:c.2385C>A	ENSP00000505996.1:p.Val795=
ENST00000680270.1:c.2442C>A	ENSP00000505532.1:p.Val814=
ENST00000680305.1:c.3144C>A	ENSP00000506312.1:p.Val1048=
ENST00000681056.1:c.2442C>A	ENSP00000506234.1:p.Val814=
ENST00000681235.1:c.*2849C>A	ENSP00000506606.1:n.*2849C>A
ENST00000681429.1:n.2995C>A
ENST00000681683.1:c.2442C>A	ENSP00000506666.1:p.Val814=
ENST00000681786.1:n.4188C>A
ENST00000681901.1:c.*2927C>A	ENSP00000504883.1:n.*2927C>A
ENST00000368471.7:c.2442C>A	ENSP00000357456.3:p.Val814=
ENST00000368474.8:c.3327C>A	ENSP00000357459.4:p.Val1109=
ENST00000492630.1:n.86C>A
ENST00000529168.1:c.3234C>A	ENSP00000431794.1:p.Val1078=
NM_001025107.2:c.2442C>A	NP_001020278.1:p.Val814=
NM_001111.4:c.3327C>A	NP_001102.2:p.Val1109=
NM_001193495.1:c.2442C>A	NP_001180424.1:p.Val814=
NM_015840.3:c.3249C>A	NP_056655.2:p.Val1083=
NM_015841.3:c.3192C>A	NP_056656.2:p.Val1064=
XM_006711109.1:c.3357C>A	XP_006711172.1:p.Val1119=
XM_006711111.2:c.2442C>A	XP_006711174.1:p.Val814=
XM_006711112.1:c.2442C>A	XP_006711175.1:p.Val814=
XM_006711113.1:c.2442C>A	XP_006711176.1:p.Val814=
XM_011509060.1:c.3456C>A	XP_011507362.1:p.Val1152=
XM_011509061.1:c.3378C>A	XP_011507363.1:p.Val1126=
XM_011509062.1:c.3345C>A	XP_011507364.1:p.Val1115=
NM_001025107.3:c.2442C>A	NP_001020278.1:p.Val814=
NM_001111.5:c.3327C>A MANE Select	NP_001102.3:p.Val1109=
NM_001193495.2:c.2442C>A	NP_001180424.1:p.Val814=
NM_001365045.1:c.3354C>A	NP_001351974.1:p.Val1118=
NM_001365046.1:c.2442C>A	NP_001351975.1:p.Val814=
NM_001365047.1:c.2442C>A	NP_001351976.1:p.Val814=
NM_001365048.1:c.2442C>A	NP_001351977.1:p.Val814=
NM_001365049.1:c.2364C>A	NP_001351978.1:p.Val788=
NM_015840.4:c.3249C>A	NP_056655.3:p.Val1083=
NM_015841.4:c.3192C>A	NP_056656.3:p.Val1064=
XM_006711113.2:c.2442C>A	XP_006711176.1:p.Val814=
XM_011509061.2:c.2364C>A	XP_011507363.2:p.Val788=
XM_024449674.1:c.3456C>A	XP_024305442.1:p.Val1152=