Canonical Allele Identifier: CA421231633

Gene: ADAR

Linked Data

• COSMIC: COSM896637 ; COSM4872792
• MyVariant Identifiers: chr1:g.154562270G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589794G>A , CM000663.2:g.154589794G>A	GRCh38
NC_000001.10:g.154562270G>A , CM000663.1:g.154562270G>A	GRCh37
NC_000001.9:g.152828894G>A	NCBI36
NG_011844.1:g.43168C>T
NG_011844.2:g.46767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2525C>T	ENSP00000497790.2:n.2525C>T
ENST00000649724.2:c.2661C>T	ENSP00000497932.2:p.Asp887=
ENST00000680270.2:c.2514C>T	ENSP00000505532.2:p.Asp838=
ENST00000681056.2:c.2283C>T	ENSP00000506234.2:p.Asp761=
ENST00000368471.8:c.1746C>T	ENSP00000357456.3:p.Asp582=
ENST00000368474.9:c.2631C>T MANE Select	ENSP00000357459.4:p.Asp877=
ENST00000529168.2:c.2553C>T	ENSP00000431794.2:p.Asp851=
ENST00000647682.2:n.2616C>T
ENST00000648231.2:c.1746C>T	ENSP00000497555.1:p.Asp582=
ENST00000648311.1:c.1746C>T	ENSP00000498137.1:p.Asp582=
ENST00000648714.2:c.*106C>T	ENSP00000497434.2:n.*106C>T
ENST00000649021.1:n.2667C>T
ENST00000649022.2:c.1746C>T	ENSP00000496896.2:p.Asp582=
ENST00000649042.1:c.1746C>T	ENSP00000497790.1:p.Asp582=
ENST00000649408.2:c.2631C>T	ENSP00000497386.2:p.Asp877=
ENST00000649724.1:c.1746C>T	ENSP00000497932.1:p.Asp582=
ENST00000649749.1:c.1746C>T	ENSP00000497210.1:p.Asp582=
ENST00000679375.1:c.*863C>T	ENSP00000505887.1:n.*863C>T
ENST00000679465.1:n.3084C>T
ENST00000679805.1:n.2667C>T
ENST00000679899.1:c.1689C>T	ENSP00000505996.1:p.Asp563=
ENST00000680270.1:c.1746C>T	ENSP00000505532.1:p.Asp582=
ENST00000680305.1:c.2631C>T	ENSP00000506312.1:p.Asp877=
ENST00000681056.1:c.1746C>T	ENSP00000506234.1:p.Asp582=
ENST00000681235.1:c.*2153C>T	ENSP00000506606.1:n.*2153C>T
ENST00000681429.1:n.1891C>T
ENST00000681683.1:c.1746C>T	ENSP00000506666.1:p.Asp582=
ENST00000681786.1:n.3084C>T
ENST00000681901.1:c.*2231C>T	ENSP00000504883.1:n.*2231C>T
ENST00000368471.7:c.1746C>T	ENSP00000357456.3:p.Asp582=
ENST00000368474.8:c.2631C>T	ENSP00000357459.4:p.Asp877=
ENST00000529168.1:c.2538C>T	ENSP00000431794.1:p.Asp846=
NM_001025107.2:c.1746C>T	NP_001020278.1:p.Asp582=
NM_001111.4:c.2631C>T	NP_001102.2:p.Asp877=
NM_001193495.1:c.1746C>T	NP_001180424.1:p.Asp582=
NM_015840.3:c.2553C>T	NP_056655.2:p.Asp851=
NM_015841.3:c.2496C>T	NP_056656.2:p.Asp832=
XM_006711109.1:c.2661C>T	XP_006711172.1:p.Asp887=
XM_006711111.2:c.1746C>T	XP_006711174.1:p.Asp582=
XM_006711112.1:c.1746C>T	XP_006711175.1:p.Asp582=
XM_006711113.1:c.1746C>T	XP_006711176.1:p.Asp582=
XM_011509060.1:c.2760C>T	XP_011507362.1:p.Asp920=
XM_011509061.1:c.2682C>T	XP_011507363.1:p.Asp894=
XM_011509062.1:c.2649C>T	XP_011507364.1:p.Asp883=
NM_001025107.3:c.1746C>T	NP_001020278.1:p.Asp582=
NM_001111.5:c.2631C>T MANE Select	NP_001102.3:p.Asp877=
NM_001193495.2:c.1746C>T	NP_001180424.1:p.Asp582=
NM_001365045.1:c.2658C>T	NP_001351974.1:p.Asp886=
NM_001365046.1:c.1746C>T	NP_001351975.1:p.Asp582=
NM_001365047.1:c.1746C>T	NP_001351976.1:p.Asp582=
NM_001365048.1:c.1746C>T	NP_001351977.1:p.Asp582=
NM_001365049.1:c.1668C>T	NP_001351978.1:p.Asp556=
NM_015840.4:c.2553C>T	NP_056655.3:p.Asp851=
NM_015841.4:c.2496C>T	NP_056656.3:p.Asp832=
XM_006711113.2:c.1746C>T	XP_006711176.1:p.Asp582=
XM_011509061.2:c.1668C>T	XP_011507363.2:p.Asp556=
XM_024449674.1:c.2760C>T	XP_024305442.1:p.Asp920=