Canonical Allele Identifier: CA421231957

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154560680A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588204A>C , CM000663.2:g.154588204A>C	GRCh38
NC_000001.10:g.154560680A>C , CM000663.1:g.154560680A>C	GRCh37
NC_000001.9:g.152827304A>C	NCBI36
NG_011844.1:g.44758T>G
NG_011844.2:g.48357T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2834T>G	ENSP00000497790.2:n.2834T>G
ENST00000649724.2:c.2970T>G	ENSP00000497932.2:p.Ala990=
ENST00000680270.2:c.2823T>G	ENSP00000505532.2:p.Ala941=
ENST00000681056.2:c.2592T>G	ENSP00000506234.2:p.Ala864=
ENST00000368471.8:c.2055T>G	ENSP00000357456.3:p.Ala685=
ENST00000368474.9:c.2940T>G MANE Select	ENSP00000357459.4:p.Ala980=
ENST00000529168.2:c.2862T>G	ENSP00000431794.2:p.Ala954=
ENST00000647682.2:n.2925T>G
ENST00000648231.2:c.2055T>G	ENSP00000497555.1:p.Ala685=
ENST00000648311.1:c.2055T>G	ENSP00000498137.1:p.Ala685=
ENST00000648714.2:c.*415T>G	ENSP00000497434.2:n.*415T>G
ENST00000649021.1:n.3268T>G
ENST00000649022.2:c.2055T>G	ENSP00000496896.2:p.Ala685=
ENST00000649042.1:c.2055T>G	ENSP00000497790.1:p.Ala685=
ENST00000649408.2:c.2940T>G	ENSP00000497386.2:p.Ala980=
ENST00000649724.1:c.2055T>G	ENSP00000497932.1:p.Ala685=
ENST00000649749.1:c.2055T>G	ENSP00000497210.1:p.Ala685=
ENST00000679375.1:c.*1172T>G	ENSP00000505887.1:n.*1172T>G
ENST00000679465.1:n.3393T>G
ENST00000679805.1:n.3268T>G
ENST00000679899.1:c.1998T>G	ENSP00000505996.1:p.Ala666=
ENST00000680270.1:c.2055T>G	ENSP00000505532.1:p.Ala685=
ENST00000680305.1:c.2940T>G	ENSP00000506312.1:p.Ala980=
ENST00000681056.1:c.2055T>G	ENSP00000506234.1:p.Ala685=
ENST00000681235.1:c.*2462T>G	ENSP00000506606.1:n.*2462T>G
ENST00000681429.1:n.2200T>G
ENST00000681683.1:c.2055T>G	ENSP00000506666.1:p.Ala685=
ENST00000681786.1:n.3393T>G
ENST00000681901.1:c.*2540T>G	ENSP00000504883.1:n.*2540T>G
ENST00000368471.7:c.2055T>G	ENSP00000357456.3:p.Ala685=
ENST00000368474.8:c.2940T>G	ENSP00000357459.4:p.Ala980=
ENST00000529168.1:c.2847T>G	ENSP00000431794.1:p.Ala949=
ENST00000530954.1:n.77T>G
ENST00000534279.1:n.399T>G
NM_001025107.2:c.2055T>G	NP_001020278.1:p.Ala685=
NM_001111.4:c.2940T>G	NP_001102.2:p.Ala980=
NM_001193495.1:c.2055T>G	NP_001180424.1:p.Ala685=
NM_015840.3:c.2862T>G	NP_056655.2:p.Ala954=
NM_015841.3:c.2805T>G	NP_056656.2:p.Ala935=
XM_006711109.1:c.2970T>G	XP_006711172.1:p.Ala990=
XM_006711111.2:c.2055T>G	XP_006711174.1:p.Ala685=
XM_006711112.1:c.2055T>G	XP_006711175.1:p.Ala685=
XM_006711113.1:c.2055T>G	XP_006711176.1:p.Ala685=
XM_011509060.1:c.3069T>G	XP_011507362.1:p.Ala1023=
XM_011509061.1:c.2991T>G	XP_011507363.1:p.Ala997=
XM_011509062.1:c.2958T>G	XP_011507364.1:p.Ala986=
NM_001025107.3:c.2055T>G	NP_001020278.1:p.Ala685=
NM_001111.5:c.2940T>G MANE Select	NP_001102.3:p.Ala980=
NM_001193495.2:c.2055T>G	NP_001180424.1:p.Ala685=
NM_001365045.1:c.2967T>G	NP_001351974.1:p.Ala989=
NM_001365046.1:c.2055T>G	NP_001351975.1:p.Ala685=
NM_001365047.1:c.2055T>G	NP_001351976.1:p.Ala685=
NM_001365048.1:c.2055T>G	NP_001351977.1:p.Ala685=
NM_001365049.1:c.1977T>G	NP_001351978.1:p.Ala659=
NM_015840.4:c.2862T>G	NP_056655.3:p.Ala954=
NM_015841.4:c.2805T>G	NP_056656.3:p.Ala935=
XM_006711113.2:c.2055T>G	XP_006711176.1:p.Ala685=
XM_011509061.2:c.1977T>G	XP_011507363.2:p.Ala659=
XM_024449674.1:c.3069T>G	XP_024305442.1:p.Ala1023=