Canonical Allele Identifier: CA342636820

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562271T>A (hg19) ; chr1:g.154589795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589795T>A , CM000663.2:g.154589795T>A	GRCh38
NC_000001.10:g.154562271T>A , CM000663.1:g.154562271T>A	GRCh37
NC_000001.9:g.152828895T>A	NCBI36
NG_011844.1:g.43167A>T
NG_011844.2:g.46766A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2524A>T	ENSP00000497790.2:n.2524A>T
ENST00000649724.2:c.2660A>T	ENSP00000497932.2:p.Asp887Val
ENST00000680270.2:c.2513A>T	ENSP00000505532.2:p.Asp838Val
ENST00000681056.2:c.2282A>T	ENSP00000506234.2:p.Asp761Val
ENST00000368471.8:c.1745A>T	ENSP00000357456.3:p.Asp582Val
ENST00000368474.9:c.2630A>T MANE Select	ENSP00000357459.4:p.Asp877Val
ENST00000529168.2:c.2552A>T	ENSP00000431794.2:p.Asp851Val
ENST00000647682.2:n.2615A>T
ENST00000648231.2:c.1745A>T	ENSP00000497555.1:p.Asp582Val
ENST00000648311.1:c.1745A>T	ENSP00000498137.1:p.Asp582Val
ENST00000648714.2:c.*105A>T	ENSP00000497434.2:n.*105A>T
ENST00000649021.1:n.2666A>T
ENST00000649022.2:c.1745A>T	ENSP00000496896.2:p.Asp582Val
ENST00000649042.1:c.1745A>T	ENSP00000497790.1:p.Asp582Val
ENST00000649408.2:c.2630A>T	ENSP00000497386.2:p.Asp877Val
ENST00000649724.1:c.1745A>T	ENSP00000497932.1:p.Asp582Val
ENST00000649749.1:c.1745A>T	ENSP00000497210.1:p.Asp582Val
ENST00000679375.1:c.*862A>T	ENSP00000505887.1:n.*862A>T
ENST00000679465.1:n.3083A>T
ENST00000679805.1:n.2666A>T
ENST00000679899.1:c.1688A>T	ENSP00000505996.1:p.Asp563Val
ENST00000680270.1:c.1745A>T	ENSP00000505532.1:p.Asp582Val
ENST00000680305.1:c.2630A>T	ENSP00000506312.1:p.Asp877Val
ENST00000681056.1:c.1745A>T	ENSP00000506234.1:p.Asp582Val
ENST00000681235.1:c.*2152A>T	ENSP00000506606.1:n.*2152A>T
ENST00000681429.1:n.1890A>T
ENST00000681683.1:c.1745A>T	ENSP00000506666.1:p.Asp582Val
ENST00000681786.1:n.3083A>T
ENST00000681901.1:c.*2230A>T	ENSP00000504883.1:n.*2230A>T
ENST00000368471.7:c.1745A>T	ENSP00000357456.3:p.Asp582Val
ENST00000368474.8:c.2630A>T	ENSP00000357459.4:p.Asp877Val
ENST00000529168.1:c.2537A>T	ENSP00000431794.1:p.Asp846Val
NM_001025107.2:c.1745A>T	NP_001020278.1:p.Asp582Val
NM_001111.4:c.2630A>T	NP_001102.2:p.Asp877Val
NM_001193495.1:c.1745A>T	NP_001180424.1:p.Asp582Val
NM_015840.3:c.2552A>T	NP_056655.2:p.Asp851Val
NM_015841.3:c.2495A>T	NP_056656.2:p.Asp832Val
XM_006711109.1:c.2660A>T	XP_006711172.1:p.Asp887Val
XM_006711111.2:c.1745A>T	XP_006711174.1:p.Asp582Val
XM_006711112.1:c.1745A>T	XP_006711175.1:p.Asp582Val
XM_006711113.1:c.1745A>T	XP_006711176.1:p.Asp582Val
XM_011509060.1:c.2759A>T	XP_011507362.1:p.Asp920Val
XM_011509061.1:c.2681A>T	XP_011507363.1:p.Asp894Val
XM_011509062.1:c.2648A>T	XP_011507364.1:p.Asp883Val
NM_001025107.3:c.1745A>T	NP_001020278.1:p.Asp582Val
NM_001111.5:c.2630A>T MANE Select	NP_001102.3:p.Asp877Val
NM_001193495.2:c.1745A>T	NP_001180424.1:p.Asp582Val
NM_001365045.1:c.2657A>T	NP_001351974.1:p.Asp886Val
NM_001365046.1:c.1745A>T	NP_001351975.1:p.Asp582Val
NM_001365047.1:c.1745A>T	NP_001351976.1:p.Asp582Val
NM_001365048.1:c.1745A>T	NP_001351977.1:p.Asp582Val
NM_001365049.1:c.1667A>T	NP_001351978.1:p.Asp556Val
NM_015840.4:c.2552A>T	NP_056655.3:p.Asp851Val
NM_015841.4:c.2495A>T	NP_056656.3:p.Asp832Val
XM_006711113.2:c.1745A>T	XP_006711176.1:p.Asp582Val
XM_011509061.2:c.1667A>T	XP_011507363.2:p.Asp556Val
XM_024449674.1:c.2759A>T	XP_024305442.1:p.Asp920Val