Canonical Allele Identifier: CA1131210

Gene: ADAR

Linked Data

• dbSNP Id: rs764889694
• ExAC: 1:154562260 T / A
• gnomAD v2: 1-154562260-T-A
• gnomAD v3: 1-154589784-T-A
• gnomAD v4: 1-154589784-T-A
• MyVariant Identifiers: chr1:g.154562260T>A (hg19) ; chr1:g.154589784T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589784T>A , CM000663.2:g.154589784T>A	GRCh38
NC_000001.10:g.154562260T>A , CM000663.1:g.154562260T>A	GRCh37
NC_000001.9:g.152828884T>A	NCBI36
NG_011844.1:g.43178A>T
NG_011844.2:g.46777A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2535A>T	ENSP00000497790.2:n.2535A>T
ENST00000649724.2:c.2671A>T	ENSP00000497932.2:p.Met891Leu
ENST00000680270.2:c.2524A>T	ENSP00000505532.2:p.Met842Leu
ENST00000681056.2:c.2293A>T	ENSP00000506234.2:p.Met765Leu
ENST00000368471.8:c.1756A>T	ENSP00000357456.3:p.Met586Leu
ENST00000368474.9:c.2641A>T MANE Select	ENSP00000357459.4:p.Met881Leu
ENST00000529168.2:c.2563A>T	ENSP00000431794.2:p.Met855Leu
ENST00000647682.2:n.2626A>T
ENST00000648231.2:c.1756A>T	ENSP00000497555.1:p.Met586Leu
ENST00000648311.1:c.1756A>T	ENSP00000498137.1:p.Met586Leu
ENST00000648714.2:c.*116A>T	ENSP00000497434.2:n.*116A>T
ENST00000649021.1:n.2677A>T
ENST00000649022.2:c.1756A>T	ENSP00000496896.2:p.Met586Leu
ENST00000649042.1:c.1756A>T	ENSP00000497790.1:p.Met586Leu
ENST00000649408.2:c.2641A>T	ENSP00000497386.2:p.Met881Leu
ENST00000649724.1:c.1756A>T	ENSP00000497932.1:p.Met586Leu
ENST00000649749.1:c.1756A>T	ENSP00000497210.1:p.Met586Leu
ENST00000679375.1:c.*873A>T	ENSP00000505887.1:n.*873A>T
ENST00000679465.1:n.3094A>T
ENST00000679805.1:n.2677A>T
ENST00000679899.1:c.1699A>T	ENSP00000505996.1:p.Met567Leu
ENST00000680270.1:c.1756A>T	ENSP00000505532.1:p.Met586Leu
ENST00000680305.1:c.2641A>T	ENSP00000506312.1:p.Met881Leu
ENST00000681056.1:c.1756A>T	ENSP00000506234.1:p.Met586Leu
ENST00000681235.1:c.*2163A>T	ENSP00000506606.1:n.*2163A>T
ENST00000681429.1:n.1901A>T
ENST00000681683.1:c.1756A>T	ENSP00000506666.1:p.Met586Leu
ENST00000681786.1:n.3094A>T
ENST00000681901.1:c.*2241A>T	ENSP00000504883.1:n.*2241A>T
ENST00000368471.7:c.1756A>T	ENSP00000357456.3:p.Met586Leu
ENST00000368474.8:c.2641A>T	ENSP00000357459.4:p.Met881Leu
ENST00000529168.1:c.2548A>T	ENSP00000431794.1:p.Met850Leu
NM_001025107.2:c.1756A>T	NP_001020278.1:p.Met586Leu
NM_001111.4:c.2641A>T	NP_001102.2:p.Met881Leu
NM_001193495.1:c.1756A>T	NP_001180424.1:p.Met586Leu
NM_015840.3:c.2563A>T	NP_056655.2:p.Met855Leu
NM_015841.3:c.2506A>T	NP_056656.2:p.Met836Leu
XM_006711109.1:c.2671A>T	XP_006711172.1:p.Met891Leu
XM_006711111.2:c.1756A>T	XP_006711174.1:p.Met586Leu
XM_006711112.1:c.1756A>T	XP_006711175.1:p.Met586Leu
XM_006711113.1:c.1756A>T	XP_006711176.1:p.Met586Leu
XM_011509060.1:c.2770A>T	XP_011507362.1:p.Met924Leu
XM_011509061.1:c.2692A>T	XP_011507363.1:p.Met898Leu
XM_011509062.1:c.2659A>T	XP_011507364.1:p.Met887Leu
NM_001025107.3:c.1756A>T	NP_001020278.1:p.Met586Leu
NM_001111.5:c.2641A>T MANE Select	NP_001102.3:p.Met881Leu
NM_001193495.2:c.1756A>T	NP_001180424.1:p.Met586Leu
NM_001365045.1:c.2668A>T	NP_001351974.1:p.Met890Leu
NM_001365046.1:c.1756A>T	NP_001351975.1:p.Met586Leu
NM_001365047.1:c.1756A>T	NP_001351976.1:p.Met586Leu
NM_001365048.1:c.1756A>T	NP_001351977.1:p.Met586Leu
NM_001365049.1:c.1678A>T	NP_001351978.1:p.Met560Leu
NM_015840.4:c.2563A>T	NP_056655.3:p.Met855Leu
NM_015841.4:c.2506A>T	NP_056656.3:p.Met836Leu
XM_006711113.2:c.1756A>T	XP_006711176.1:p.Met586Leu
XM_011509061.2:c.1678A>T	XP_011507363.2:p.Met560Leu
XM_024449674.1:c.2770A>T	XP_024305442.1:p.Met924Leu