Canonical Allele Identifier: CA342636729

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589462-C-T
• MyVariant Identifiers: chr1:g.154561938C>T (hg19) ; chr1:g.154589462C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589462C>T , CM000663.2:g.154589462C>T	GRCh38
NC_000001.10:g.154561938C>T , CM000663.1:g.154561938C>T	GRCh37
NC_000001.9:g.152828562C>T	NCBI36
NG_011844.1:g.43500G>A
NG_011844.2:g.47099G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.2563G>A	ENSP00000497790.2:n.2563G>A
ENST00000649724.2:c.2699G>A	ENSP00000497932.2:p.Gly900Glu
ENST00000680270.2:c.2552G>A	ENSP00000505532.2:p.Gly851Glu
ENST00000681056.2:c.2321G>A	ENSP00000506234.2:p.Gly774Glu
ENST00000368471.8:c.1784G>A	ENSP00000357456.3:p.Gly595Glu
ENST00000368474.9:c.2669G>A MANE Select	ENSP00000357459.4:p.Gly890Glu
ENST00000529168.2:c.2591G>A	ENSP00000431794.2:p.Gly864Glu
ENST00000647682.2:n.2654G>A
ENST00000648231.2:c.1784G>A	ENSP00000497555.1:p.Gly595Glu
ENST00000648311.1:c.1784G>A	ENSP00000498137.1:p.Gly595Glu
ENST00000648714.2:c.*144G>A	ENSP00000497434.2:n.*144G>A
ENST00000649021.1:n.2705G>A
ENST00000649022.2:c.1784G>A	ENSP00000496896.2:p.Gly595Glu
ENST00000649042.1:c.1784G>A	ENSP00000497790.1:p.Gly595Glu
ENST00000649408.2:c.2669G>A	ENSP00000497386.2:p.Gly890Glu
ENST00000649724.1:c.1784G>A	ENSP00000497932.1:p.Gly595Glu
ENST00000649749.1:c.1784G>A	ENSP00000497210.1:p.Gly595Glu
ENST00000679375.1:c.*901G>A	ENSP00000505887.1:n.*901G>A
ENST00000679465.1:n.3122G>A
ENST00000679805.1:n.2705G>A
ENST00000679899.1:c.1727G>A	ENSP00000505996.1:p.Gly576Glu
ENST00000680270.1:c.1784G>A	ENSP00000505532.1:p.Gly595Glu
ENST00000680305.1:c.2669G>A	ENSP00000506312.1:p.Gly890Glu
ENST00000681056.1:c.1784G>A	ENSP00000506234.1:p.Gly595Glu
ENST00000681235.1:c.*2191G>A	ENSP00000506606.1:n.*2191G>A
ENST00000681429.1:n.1929G>A
ENST00000681683.1:c.1784G>A	ENSP00000506666.1:p.Gly595Glu
ENST00000681786.1:n.3122G>A
ENST00000681901.1:c.*2269G>A	ENSP00000504883.1:n.*2269G>A
ENST00000368471.7:c.1784G>A	ENSP00000357456.3:p.Gly595Glu
ENST00000368474.8:c.2669G>A	ENSP00000357459.4:p.Gly890Glu
ENST00000529168.1:c.2576G>A	ENSP00000431794.1:p.Gly859Glu
NM_001025107.2:c.1784G>A	NP_001020278.1:p.Gly595Glu
NM_001111.4:c.2669G>A	NP_001102.2:p.Gly890Glu
NM_001193495.1:c.1784G>A	NP_001180424.1:p.Gly595Glu
NM_015840.3:c.2591G>A	NP_056655.2:p.Gly864Glu
NM_015841.3:c.2534G>A	NP_056656.2:p.Gly845Glu
XM_006711109.1:c.2699G>A	XP_006711172.1:p.Gly900Glu
XM_006711111.2:c.1784G>A	XP_006711174.1:p.Gly595Glu
XM_006711112.1:c.1784G>A	XP_006711175.1:p.Gly595Glu
XM_006711113.1:c.1784G>A	XP_006711176.1:p.Gly595Glu
XM_011509060.1:c.2798G>A	XP_011507362.1:p.Gly933Glu
XM_011509061.1:c.2720G>A	XP_011507363.1:p.Gly907Glu
XM_011509062.1:c.2687G>A	XP_011507364.1:p.Gly896Glu
NM_001025107.3:c.1784G>A	NP_001020278.1:p.Gly595Glu
NM_001111.5:c.2669G>A MANE Select	NP_001102.3:p.Gly890Glu
NM_001193495.2:c.1784G>A	NP_001180424.1:p.Gly595Glu
NM_001365045.1:c.2696G>A	NP_001351974.1:p.Gly899Glu
NM_001365046.1:c.1784G>A	NP_001351975.1:p.Gly595Glu
NM_001365047.1:c.1784G>A	NP_001351976.1:p.Gly595Glu
NM_001365048.1:c.1784G>A	NP_001351977.1:p.Gly595Glu
NM_001365049.1:c.1706G>A	NP_001351978.1:p.Gly569Glu
NM_015840.4:c.2591G>A	NP_056655.3:p.Gly864Glu
NM_015841.4:c.2534G>A	NP_056656.3:p.Gly845Glu
XM_006711113.2:c.1784G>A	XP_006711176.1:p.Gly595Glu
XM_011509061.2:c.1706G>A	XP_011507363.2:p.Gly569Glu
XM_024449674.1:c.2798G>A	XP_024305442.1:p.Gly933Glu