Canonical Allele Identifier: CA342636772

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562247A>G (hg19) ; chr1:g.154589771A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589771A>G , CM000663.2:g.154589771A>G	GRCh38
NC_000001.10:g.154562247A>G , CM000663.1:g.154562247A>G	GRCh37
NC_000001.9:g.152828871A>G	NCBI36
NG_011844.1:g.43191T>C
NG_011844.2:g.46790T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2548T>C	ENSP00000497790.2:n.2548T>C
ENST00000649724.2:c.2684T>C	ENSP00000497932.2:p.Val895Ala
ENST00000680270.2:c.2537T>C	ENSP00000505532.2:p.Val846Ala
ENST00000681056.2:c.2306T>C	ENSP00000506234.2:p.Val769Ala
ENST00000368471.8:c.1769T>C	ENSP00000357456.3:p.Val590Ala
ENST00000368474.9:c.2654T>C MANE Select	ENSP00000357459.4:p.Val885Ala
ENST00000529168.2:c.2576T>C	ENSP00000431794.2:p.Val859Ala
ENST00000647682.2:n.2639T>C
ENST00000648231.2:c.1769T>C	ENSP00000497555.1:p.Val590Ala
ENST00000648311.1:c.1769T>C	ENSP00000498137.1:p.Val590Ala
ENST00000648714.2:c.*129T>C	ENSP00000497434.2:n.*129T>C
ENST00000649021.1:n.2690T>C
ENST00000649022.2:c.1769T>C	ENSP00000496896.2:p.Val590Ala
ENST00000649042.1:c.1769T>C	ENSP00000497790.1:p.Val590Ala
ENST00000649408.2:c.2654T>C	ENSP00000497386.2:p.Val885Ala
ENST00000649724.1:c.1769T>C	ENSP00000497932.1:p.Val590Ala
ENST00000649749.1:c.1769T>C	ENSP00000497210.1:p.Val590Ala
ENST00000679375.1:c.*886T>C	ENSP00000505887.1:n.*886T>C
ENST00000679465.1:n.3107T>C
ENST00000679805.1:n.2690T>C
ENST00000679899.1:c.1712T>C	ENSP00000505996.1:p.Val571Ala
ENST00000680270.1:c.1769T>C	ENSP00000505532.1:p.Val590Ala
ENST00000680305.1:c.2654T>C	ENSP00000506312.1:p.Val885Ala
ENST00000681056.1:c.1769T>C	ENSP00000506234.1:p.Val590Ala
ENST00000681235.1:c.*2176T>C	ENSP00000506606.1:n.*2176T>C
ENST00000681429.1:n.1914T>C
ENST00000681683.1:c.1769T>C	ENSP00000506666.1:p.Val590Ala
ENST00000681786.1:n.3107T>C
ENST00000681901.1:c.*2254T>C	ENSP00000504883.1:n.*2254T>C
ENST00000368471.7:c.1769T>C	ENSP00000357456.3:p.Val590Ala
ENST00000368474.8:c.2654T>C	ENSP00000357459.4:p.Val885Ala
ENST00000529168.1:c.2561T>C	ENSP00000431794.1:p.Val854Ala
NM_001025107.2:c.1769T>C	NP_001020278.1:p.Val590Ala
NM_001111.4:c.2654T>C	NP_001102.2:p.Val885Ala
NM_001193495.1:c.1769T>C	NP_001180424.1:p.Val590Ala
NM_015840.3:c.2576T>C	NP_056655.2:p.Val859Ala
NM_015841.3:c.2519T>C	NP_056656.2:p.Val840Ala
XM_006711109.1:c.2684T>C	XP_006711172.1:p.Val895Ala
XM_006711111.2:c.1769T>C	XP_006711174.1:p.Val590Ala
XM_006711112.1:c.1769T>C	XP_006711175.1:p.Val590Ala
XM_006711113.1:c.1769T>C	XP_006711176.1:p.Val590Ala
XM_011509060.1:c.2783T>C	XP_011507362.1:p.Val928Ala
XM_011509061.1:c.2705T>C	XP_011507363.1:p.Val902Ala
XM_011509062.1:c.2672T>C	XP_011507364.1:p.Val891Ala
NM_001025107.3:c.1769T>C	NP_001020278.1:p.Val590Ala
NM_001111.5:c.2654T>C MANE Select	NP_001102.3:p.Val885Ala
NM_001193495.2:c.1769T>C	NP_001180424.1:p.Val590Ala
NM_001365045.1:c.2681T>C	NP_001351974.1:p.Val894Ala
NM_001365046.1:c.1769T>C	NP_001351975.1:p.Val590Ala
NM_001365047.1:c.1769T>C	NP_001351976.1:p.Val590Ala
NM_001365048.1:c.1769T>C	NP_001351977.1:p.Val590Ala
NM_001365049.1:c.1691T>C	NP_001351978.1:p.Val564Ala
NM_015840.4:c.2576T>C	NP_056655.3:p.Val859Ala
NM_015841.4:c.2519T>C	NP_056656.3:p.Val840Ala
XM_006711113.2:c.1769T>C	XP_006711176.1:p.Val590Ala
XM_011509061.2:c.1691T>C	XP_011507363.2:p.Val564Ala
XM_024449674.1:c.2783T>C	XP_024305442.1:p.Val928Ala