Canonical Allele Identifier: CA342603925

Gene: ADAR

Linked Data

• ClinVar Variation Id: 2085862
• ClinVar RCV Id: RCV003005295
• gnomAD v4: 1-154602277-C-T
• MyVariant Identifiers: chr1:g.154574753C>T (hg19) ; chr1:g.154602277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602277C>T , CM000663.2:g.154602277C>T	GRCh38
NC_000001.10:g.154574753C>T , CM000663.1:g.154574753C>T	GRCh37
NC_000001.9:g.152841377C>T	NCBI36
NG_011844.1:g.30685G>A
NG_011844.2:g.34284G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.288-29G>A	ENSP00000497790.2:n.288-29G>A
ENST00000649724.2:c.395G>A	ENSP00000497932.2:p.Gly132Asp
ENST00000680270.2:c.395G>A	ENSP00000505532.2:p.Gly132Asp
ENST00000681056.2:c.46-29G>A	ENSP00000506234.2:n.46-29G>A
ENST00000368471.8:c.-521G>A	ENSP00000357456.3:n.-521G>A
ENST00000368474.9:c.365G>A MANE Select	ENSP00000357459.4:p.Gly122Asp
ENST00000471068.2:n.391-29G>A
ENST00000526905.2:n.258-29G>A
ENST00000529168.2:c.365G>A	ENSP00000431794.2:p.Gly122Asp
ENST00000647682.2:n.124-29G>A
ENST00000648231.2:c.-521G>A	ENSP00000497555.1:n.-521G>A
ENST00000648311.1:c.-521G>A	ENSP00000498137.1:n.-521G>A
ENST00000648714.2:c.365G>A	ENSP00000497434.2:p.Gly122Asp
ENST00000648871.1:c.-492-29G>A	ENSP00000497793.1:n.-492-29G>A
ENST00000649021.1:n.401G>A
ENST00000649022.2:c.-521G>A	ENSP00000496896.2:n.-521G>A
ENST00000649042.1:c.-492-29G>A	ENSP00000497790.1:n.-492-29G>A
ENST00000649408.2:c.365G>A	ENSP00000497386.2:p.Gly122Asp
ENST00000649724.1:c.-521G>A	ENSP00000497932.1:n.-521G>A
ENST00000649749.1:c.-521G>A	ENSP00000497210.1:n.-521G>A
ENST00000679375.1:c.-492-29G>A	ENSP00000505887.1:n.-492-29G>A
ENST00000679465.1:n.563G>A
ENST00000679805.1:n.401G>A
ENST00000679899.1:c.-521G>A	ENSP00000505996.1:n.-521G>A
ENST00000680270.1:c.-374G>A	ENSP00000505532.1:n.-374G>A
ENST00000680305.1:c.365G>A	ENSP00000506312.1:p.Gly122Asp
ENST00000680472.1:n.404G>A
ENST00000681056.1:c.-492-29G>A	ENSP00000506234.1:n.-492-29G>A
ENST00000681235.1:c.258-29G>A	ENSP00000506606.1:n.258-29G>A
ENST00000681683.1:c.-492-29G>A	ENSP00000506666.1:n.-492-29G>A
ENST00000681786.1:n.563G>A
ENST00000681901.1:c.258-29G>A	ENSP00000504883.1:n.258-29G>A
ENST00000368471.7:c.-521G>A	ENSP00000357456.3:n.-521G>A
ENST00000368474.8:c.365G>A	ENSP00000357459.4:p.Gly122Asp
ENST00000463920.5:n.276-29G>A
ENST00000471068.1:n.396G>A
ENST00000494866.1:n.301-29G>A
ENST00000526905.1:n.412G>A
ENST00000529168.1:c.350G>A	ENSP00000431794.1:p.Gly117Asp
NM_001025107.2:c.-521G>A	NP_001020278.1:n.-521G>A
NM_001111.4:c.365G>A	NP_001102.2:p.Gly122Asp
NM_001193495.1:c.-521G>A	NP_001180424.1:n.-521G>A
NM_015840.3:c.365G>A	NP_056655.2:p.Gly122Asp
NM_015841.3:c.365G>A	NP_056656.2:p.Gly122Asp
XM_006711109.1:c.395G>A	XP_006711172.1:p.Gly132Asp
XM_006711111.2:c.-492-29G>A	XP_006711174.1:n.-492-29G>A
XM_006711112.1:c.-492-29G>A	XP_006711175.1:n.-492-29G>A
XM_006711113.1:c.-492-29G>A	XP_006711176.1:n.-492-29G>A
XM_011509060.1:c.494G>A	XP_011507362.1:p.Gly165Asp
XM_011509061.1:c.494G>A	XP_011507363.1:p.Gly165Asp
XM_011509062.1:c.383G>A	XP_011507364.1:p.Gly128Asp
NM_001025107.3:c.-521G>A	NP_001020278.1:n.-521G>A
NM_001111.5:c.365G>A MANE Select	NP_001102.3:p.Gly122Asp
NM_001193495.2:c.-521G>A	NP_001180424.1:n.-521G>A
NM_001365045.1:c.392G>A	NP_001351974.1:p.Gly131Asp
NM_001365046.1:c.-492-29G>A	NP_001351975.1:n.-492-29G>A
NM_001365047.1:c.-492-29G>A	NP_001351976.1:n.-492-29G>A
NM_001365048.1:c.-521G>A	NP_001351977.1:n.-521G>A
NM_001365049.1:c.-492-29G>A	NP_001351978.1:n.-492-29G>A
NM_015840.4:c.365G>A	NP_056655.3:p.Gly122Asp
NM_015841.4:c.365G>A	NP_056656.3:p.Gly122Asp
XM_006711113.2:c.-492-29G>A	XP_006711176.1:n.-492-29G>A
XM_011509061.2:c.-521G>A	XP_011507363.2:n.-521G>A
XM_024449674.1:c.494G>A	XP_024305442.1:p.Gly165Asp