Canonical Allele Identifier: CA342636522

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154561845C>A (hg19) ; chr1:g.154589369C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589369C>A , CM000663.2:g.154589369C>A	GRCh38
NC_000001.10:g.154561845C>A , CM000663.1:g.154561845C>A	GRCh37
NC_000001.9:g.152828469C>A	NCBI36
NG_011844.1:g.43593G>T
NG_011844.2:g.47192G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.2656G>T	ENSP00000497790.2:n.2656G>T
ENST00000649724.2:c.2792G>T	ENSP00000497932.2:p.Arg931Met
ENST00000680270.2:c.2645G>T	ENSP00000505532.2:p.Arg882Met
ENST00000681056.2:c.2414G>T	ENSP00000506234.2:p.Arg805Met
ENST00000368471.8:c.1877G>T	ENSP00000357456.3:p.Arg626Met
ENST00000368474.9:c.2762G>T MANE Select	ENSP00000357459.4:p.Arg921Met
ENST00000529168.2:c.2684G>T	ENSP00000431794.2:p.Arg895Met
ENST00000647682.2:n.2747G>T
ENST00000648231.2:c.1877G>T	ENSP00000497555.1:p.Arg626Met
ENST00000648311.1:c.1877G>T	ENSP00000498137.1:p.Arg626Met
ENST00000648714.2:c.*237G>T	ENSP00000497434.2:n.*237G>T
ENST00000649021.1:n.2798G>T
ENST00000649022.2:c.1877G>T	ENSP00000496896.2:p.Arg626Met
ENST00000649042.1:c.1877G>T	ENSP00000497790.1:p.Arg626Met
ENST00000649408.2:c.2762G>T	ENSP00000497386.2:p.Arg921Met
ENST00000649724.1:c.1877G>T	ENSP00000497932.1:p.Arg626Met
ENST00000649749.1:c.1877G>T	ENSP00000497210.1:p.Arg626Met
ENST00000679375.1:c.*994G>T	ENSP00000505887.1:n.*994G>T
ENST00000679465.1:n.3215G>T
ENST00000679805.1:n.2798G>T
ENST00000679899.1:c.1820G>T	ENSP00000505996.1:p.Arg607Met
ENST00000680270.1:c.1877G>T	ENSP00000505532.1:p.Arg626Met
ENST00000680305.1:c.2762G>T	ENSP00000506312.1:p.Arg921Met
ENST00000681056.1:c.1877G>T	ENSP00000506234.1:p.Arg626Met
ENST00000681235.1:c.*2284G>T	ENSP00000506606.1:n.*2284G>T
ENST00000681429.1:n.2022G>T
ENST00000681683.1:c.1877G>T	ENSP00000506666.1:p.Arg626Met
ENST00000681786.1:n.3215G>T
ENST00000681901.1:c.*2362G>T	ENSP00000504883.1:n.*2362G>T
ENST00000368471.7:c.1877G>T	ENSP00000357456.3:p.Arg626Met
ENST00000368474.8:c.2762G>T	ENSP00000357459.4:p.Arg921Met
ENST00000529168.1:c.2669G>T	ENSP00000431794.1:p.Arg890Met
NM_001025107.2:c.1877G>T	NP_001020278.1:p.Arg626Met
NM_001111.4:c.2762G>T	NP_001102.2:p.Arg921Met
NM_001193495.1:c.1877G>T	NP_001180424.1:p.Arg626Met
NM_015840.3:c.2684G>T	NP_056655.2:p.Arg895Met
NM_015841.3:c.2627G>T	NP_056656.2:p.Arg876Met
XM_006711109.1:c.2792G>T	XP_006711172.1:p.Arg931Met
XM_006711111.2:c.1877G>T	XP_006711174.1:p.Arg626Met
XM_006711112.1:c.1877G>T	XP_006711175.1:p.Arg626Met
XM_006711113.1:c.1877G>T	XP_006711176.1:p.Arg626Met
XM_011509060.1:c.2891G>T	XP_011507362.1:p.Arg964Met
XM_011509061.1:c.2813G>T	XP_011507363.1:p.Arg938Met
XM_011509062.1:c.2780G>T	XP_011507364.1:p.Arg927Met
NM_001025107.3:c.1877G>T	NP_001020278.1:p.Arg626Met
NM_001111.5:c.2762G>T MANE Select	NP_001102.3:p.Arg921Met
NM_001193495.2:c.1877G>T	NP_001180424.1:p.Arg626Met
NM_001365045.1:c.2789G>T	NP_001351974.1:p.Arg930Met
NM_001365046.1:c.1877G>T	NP_001351975.1:p.Arg626Met
NM_001365047.1:c.1877G>T	NP_001351976.1:p.Arg626Met
NM_001365048.1:c.1877G>T	NP_001351977.1:p.Arg626Met
NM_001365049.1:c.1799G>T	NP_001351978.1:p.Arg600Met
NM_015840.4:c.2684G>T	NP_056655.3:p.Arg895Met
NM_015841.4:c.2627G>T	NP_056656.3:p.Arg876Met
XM_006711113.2:c.1877G>T	XP_006711176.1:p.Arg626Met
XM_011509061.2:c.1799G>T	XP_011507363.2:p.Arg600Met
XM_024449674.1:c.2891G>T	XP_024305442.1:p.Arg964Met