Canonical Allele Identifier: CA421225782

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154574749A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602273A>C , CM000663.2:g.154602273A>C	GRCh38
NC_000001.10:g.154574749A>C , CM000663.1:g.154574749A>C	GRCh37
NC_000001.9:g.152841373A>C	NCBI36
NG_011844.1:g.30689T>G
NG_011844.2:g.34288T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.288-25T>G	ENSP00000497790.2:n.288-25T>G
ENST00000649724.2:c.399T>G	ENSP00000497932.2:p.Val133=
ENST00000680270.2:c.399T>G	ENSP00000505532.2:p.Val133=
ENST00000681056.2:c.46-25T>G	ENSP00000506234.2:n.46-25T>G
ENST00000368471.8:c.-517T>G	ENSP00000357456.3:n.-517T>G
ENST00000368474.9:c.369T>G MANE Select	ENSP00000357459.4:p.Val123=
ENST00000471068.2:n.391-25T>G
ENST00000526905.2:n.258-25T>G
ENST00000529168.2:c.369T>G	ENSP00000431794.2:p.Val123=
ENST00000647682.2:n.124-25T>G
ENST00000648231.2:c.-517T>G	ENSP00000497555.1:n.-517T>G
ENST00000648311.1:c.-517T>G	ENSP00000498137.1:n.-517T>G
ENST00000648714.2:c.369T>G	ENSP00000497434.2:p.Val123=
ENST00000648871.1:c.-492-25T>G	ENSP00000497793.1:n.-492-25T>G
ENST00000649021.1:n.405T>G
ENST00000649022.2:c.-517T>G	ENSP00000496896.2:n.-517T>G
ENST00000649042.1:c.-492-25T>G	ENSP00000497790.1:n.-492-25T>G
ENST00000649408.2:c.369T>G	ENSP00000497386.2:p.Val123=
ENST00000649724.1:c.-517T>G	ENSP00000497932.1:n.-517T>G
ENST00000649749.1:c.-517T>G	ENSP00000497210.1:n.-517T>G
ENST00000679375.1:c.-492-25T>G	ENSP00000505887.1:n.-492-25T>G
ENST00000679465.1:n.567T>G
ENST00000679805.1:n.405T>G
ENST00000679899.1:c.-517T>G	ENSP00000505996.1:n.-517T>G
ENST00000680270.1:c.-370T>G	ENSP00000505532.1:n.-370T>G
ENST00000680305.1:c.369T>G	ENSP00000506312.1:p.Val123=
ENST00000680472.1:n.408T>G
ENST00000681056.1:c.-492-25T>G	ENSP00000506234.1:n.-492-25T>G
ENST00000681235.1:c.258-25T>G	ENSP00000506606.1:n.258-25T>G
ENST00000681683.1:c.-492-25T>G	ENSP00000506666.1:n.-492-25T>G
ENST00000681786.1:n.567T>G
ENST00000681901.1:c.258-25T>G	ENSP00000504883.1:n.258-25T>G
ENST00000368471.7:c.-517T>G	ENSP00000357456.3:n.-517T>G
ENST00000368474.8:c.369T>G	ENSP00000357459.4:p.Val123=
ENST00000463920.5:n.276-25T>G
ENST00000471068.1:n.400T>G
ENST00000494866.1:n.301-25T>G
ENST00000526905.1:n.416T>G
ENST00000529168.1:c.354T>G	ENSP00000431794.1:p.Val118=
NM_001025107.2:c.-517T>G	NP_001020278.1:n.-517T>G
NM_001111.4:c.369T>G	NP_001102.2:p.Val123=
NM_001193495.1:c.-517T>G	NP_001180424.1:n.-517T>G
NM_015840.3:c.369T>G	NP_056655.2:p.Val123=
NM_015841.3:c.369T>G	NP_056656.2:p.Val123=
XM_006711109.1:c.399T>G	XP_006711172.1:p.Val133=
XM_006711111.2:c.-492-25T>G	XP_006711174.1:n.-492-25T>G
XM_006711112.1:c.-492-25T>G	XP_006711175.1:n.-492-25T>G
XM_006711113.1:c.-492-25T>G	XP_006711176.1:n.-492-25T>G
XM_011509060.1:c.498T>G	XP_011507362.1:p.Val166=
XM_011509061.1:c.498T>G	XP_011507363.1:p.Val166=
XM_011509062.1:c.387T>G	XP_011507364.1:p.Val129=
NM_001025107.3:c.-517T>G	NP_001020278.1:n.-517T>G
NM_001111.5:c.369T>G MANE Select	NP_001102.3:p.Val123=
NM_001193495.2:c.-517T>G	NP_001180424.1:n.-517T>G
NM_001365045.1:c.396T>G	NP_001351974.1:p.Val132=
NM_001365046.1:c.-492-25T>G	NP_001351975.1:n.-492-25T>G
NM_001365047.1:c.-492-25T>G	NP_001351976.1:n.-492-25T>G
NM_001365048.1:c.-517T>G	NP_001351977.1:n.-517T>G
NM_001365049.1:c.-492-25T>G	NP_001351978.1:n.-492-25T>G
NM_015840.4:c.369T>G	NP_056655.3:p.Val123=
NM_015841.4:c.369T>G	NP_056656.3:p.Val123=
XM_006711113.2:c.-492-25T>G	XP_006711176.1:n.-492-25T>G
XM_011509061.2:c.-517T>G	XP_011507363.2:n.-517T>G
XM_024449674.1:c.498T>G	XP_024305442.1:p.Val166=