Canonical Allele Identifier: CA342636665

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154561909T>G (hg19) ; chr1:g.154589433T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589433T>G , CM000663.2:g.154589433T>G	GRCh38
NC_000001.10:g.154561909T>G , CM000663.1:g.154561909T>G	GRCh37
NC_000001.9:g.152828533T>G	NCBI36
NG_011844.1:g.43529A>C
NG_011844.2:g.47128A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2592A>C	ENSP00000497790.2:n.2592A>C
ENST00000649724.2:c.2728A>C	ENSP00000497932.2:p.Ser910Arg
ENST00000680270.2:c.2581A>C	ENSP00000505532.2:p.Ser861Arg
ENST00000681056.2:c.2350A>C	ENSP00000506234.2:p.Ser784Arg
ENST00000368471.8:c.1813A>C	ENSP00000357456.3:p.Ser605Arg
ENST00000368474.9:c.2698A>C MANE Select	ENSP00000357459.4:p.Ser900Arg
ENST00000529168.2:c.2620A>C	ENSP00000431794.2:p.Ser874Arg
ENST00000647682.2:n.2683A>C
ENST00000648231.2:c.1813A>C	ENSP00000497555.1:p.Ser605Arg
ENST00000648311.1:c.1813A>C	ENSP00000498137.1:p.Ser605Arg
ENST00000648714.2:c.*173A>C	ENSP00000497434.2:n.*173A>C
ENST00000649021.1:n.2734A>C
ENST00000649022.2:c.1813A>C	ENSP00000496896.2:p.Ser605Arg
ENST00000649042.1:c.1813A>C	ENSP00000497790.1:p.Ser605Arg
ENST00000649408.2:c.2698A>C	ENSP00000497386.2:p.Ser900Arg
ENST00000649724.1:c.1813A>C	ENSP00000497932.1:p.Ser605Arg
ENST00000649749.1:c.1813A>C	ENSP00000497210.1:p.Ser605Arg
ENST00000679375.1:c.*930A>C	ENSP00000505887.1:n.*930A>C
ENST00000679465.1:n.3151A>C
ENST00000679805.1:n.2734A>C
ENST00000679899.1:c.1756A>C	ENSP00000505996.1:p.Ser586Arg
ENST00000680270.1:c.1813A>C	ENSP00000505532.1:p.Ser605Arg
ENST00000680305.1:c.2698A>C	ENSP00000506312.1:p.Ser900Arg
ENST00000681056.1:c.1813A>C	ENSP00000506234.1:p.Ser605Arg
ENST00000681235.1:c.*2220A>C	ENSP00000506606.1:n.*2220A>C
ENST00000681429.1:n.1958A>C
ENST00000681683.1:c.1813A>C	ENSP00000506666.1:p.Ser605Arg
ENST00000681786.1:n.3151A>C
ENST00000681901.1:c.*2298A>C	ENSP00000504883.1:n.*2298A>C
ENST00000368471.7:c.1813A>C	ENSP00000357456.3:p.Ser605Arg
ENST00000368474.8:c.2698A>C	ENSP00000357459.4:p.Ser900Arg
ENST00000529168.1:c.2605A>C	ENSP00000431794.1:p.Ser869Arg
NM_001025107.2:c.1813A>C	NP_001020278.1:p.Ser605Arg
NM_001111.4:c.2698A>C	NP_001102.2:p.Ser900Arg
NM_001193495.1:c.1813A>C	NP_001180424.1:p.Ser605Arg
NM_015840.3:c.2620A>C	NP_056655.2:p.Ser874Arg
NM_015841.3:c.2563A>C	NP_056656.2:p.Ser855Arg
XM_006711109.1:c.2728A>C	XP_006711172.1:p.Ser910Arg
XM_006711111.2:c.1813A>C	XP_006711174.1:p.Ser605Arg
XM_006711112.1:c.1813A>C	XP_006711175.1:p.Ser605Arg
XM_006711113.1:c.1813A>C	XP_006711176.1:p.Ser605Arg
XM_011509060.1:c.2827A>C	XP_011507362.1:p.Ser943Arg
XM_011509061.1:c.2749A>C	XP_011507363.1:p.Ser917Arg
XM_011509062.1:c.2716A>C	XP_011507364.1:p.Ser906Arg
NM_001025107.3:c.1813A>C	NP_001020278.1:p.Ser605Arg
NM_001111.5:c.2698A>C MANE Select	NP_001102.3:p.Ser900Arg
NM_001193495.2:c.1813A>C	NP_001180424.1:p.Ser605Arg
NM_001365045.1:c.2725A>C	NP_001351974.1:p.Ser909Arg
NM_001365046.1:c.1813A>C	NP_001351975.1:p.Ser605Arg
NM_001365047.1:c.1813A>C	NP_001351976.1:p.Ser605Arg
NM_001365048.1:c.1813A>C	NP_001351977.1:p.Ser605Arg
NM_001365049.1:c.1735A>C	NP_001351978.1:p.Ser579Arg
NM_015840.4:c.2620A>C	NP_056655.3:p.Ser874Arg
NM_015841.4:c.2563A>C	NP_056656.3:p.Ser855Arg
XM_006711113.2:c.1813A>C	XP_006711176.1:p.Ser605Arg
XM_011509061.2:c.1735A>C	XP_011507363.2:p.Ser579Arg
XM_024449674.1:c.2827A>C	XP_024305442.1:p.Ser943Arg