Canonical Allele Identifier: CA342636651

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154561903T>C (hg19) ; chr1:g.154589427T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589427T>C , CM000663.2:g.154589427T>C	GRCh38
NC_000001.10:g.154561903T>C , CM000663.1:g.154561903T>C	GRCh37
NC_000001.9:g.152828527T>C	NCBI36
NG_011844.1:g.43535A>G
NG_011844.2:g.47134A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2598A>G	ENSP00000497790.2:n.2598A>G
ENST00000649724.2:c.2734A>G	ENSP00000497932.2:p.Lys912Glu
ENST00000680270.2:c.2587A>G	ENSP00000505532.2:p.Lys863Glu
ENST00000681056.2:c.2356A>G	ENSP00000506234.2:p.Lys786Glu
ENST00000368471.8:c.1819A>G	ENSP00000357456.3:p.Lys607Glu
ENST00000368474.9:c.2704A>G MANE Select	ENSP00000357459.4:p.Lys902Glu
ENST00000529168.2:c.2626A>G	ENSP00000431794.2:p.Lys876Glu
ENST00000647682.2:n.2689A>G
ENST00000648231.2:c.1819A>G	ENSP00000497555.1:p.Lys607Glu
ENST00000648311.1:c.1819A>G	ENSP00000498137.1:p.Lys607Glu
ENST00000648714.2:c.*179A>G	ENSP00000497434.2:n.*179A>G
ENST00000649021.1:n.2740A>G
ENST00000649022.2:c.1819A>G	ENSP00000496896.2:p.Lys607Glu
ENST00000649042.1:c.1819A>G	ENSP00000497790.1:p.Lys607Glu
ENST00000649408.2:c.2704A>G	ENSP00000497386.2:p.Lys902Glu
ENST00000649724.1:c.1819A>G	ENSP00000497932.1:p.Lys607Glu
ENST00000649749.1:c.1819A>G	ENSP00000497210.1:p.Lys607Glu
ENST00000679375.1:c.*936A>G	ENSP00000505887.1:n.*936A>G
ENST00000679465.1:n.3157A>G
ENST00000679805.1:n.2740A>G
ENST00000679899.1:c.1762A>G	ENSP00000505996.1:p.Lys588Glu
ENST00000680270.1:c.1819A>G	ENSP00000505532.1:p.Lys607Glu
ENST00000680305.1:c.2704A>G	ENSP00000506312.1:p.Lys902Glu
ENST00000681056.1:c.1819A>G	ENSP00000506234.1:p.Lys607Glu
ENST00000681235.1:c.*2226A>G	ENSP00000506606.1:n.*2226A>G
ENST00000681429.1:n.1964A>G
ENST00000681683.1:c.1819A>G	ENSP00000506666.1:p.Lys607Glu
ENST00000681786.1:n.3157A>G
ENST00000681901.1:c.*2304A>G	ENSP00000504883.1:n.*2304A>G
ENST00000368471.7:c.1819A>G	ENSP00000357456.3:p.Lys607Glu
ENST00000368474.8:c.2704A>G	ENSP00000357459.4:p.Lys902Glu
ENST00000529168.1:c.2611A>G	ENSP00000431794.1:p.Lys871Glu
NM_001025107.2:c.1819A>G	NP_001020278.1:p.Lys607Glu
NM_001111.4:c.2704A>G	NP_001102.2:p.Lys902Glu
NM_001193495.1:c.1819A>G	NP_001180424.1:p.Lys607Glu
NM_015840.3:c.2626A>G	NP_056655.2:p.Lys876Glu
NM_015841.3:c.2569A>G	NP_056656.2:p.Lys857Glu
XM_006711109.1:c.2734A>G	XP_006711172.1:p.Lys912Glu
XM_006711111.2:c.1819A>G	XP_006711174.1:p.Lys607Glu
XM_006711112.1:c.1819A>G	XP_006711175.1:p.Lys607Glu
XM_006711113.1:c.1819A>G	XP_006711176.1:p.Lys607Glu
XM_011509060.1:c.2833A>G	XP_011507362.1:p.Lys945Glu
XM_011509061.1:c.2755A>G	XP_011507363.1:p.Lys919Glu
XM_011509062.1:c.2722A>G	XP_011507364.1:p.Lys908Glu
NM_001025107.3:c.1819A>G	NP_001020278.1:p.Lys607Glu
NM_001111.5:c.2704A>G MANE Select	NP_001102.3:p.Lys902Glu
NM_001193495.2:c.1819A>G	NP_001180424.1:p.Lys607Glu
NM_001365045.1:c.2731A>G	NP_001351974.1:p.Lys911Glu
NM_001365046.1:c.1819A>G	NP_001351975.1:p.Lys607Glu
NM_001365047.1:c.1819A>G	NP_001351976.1:p.Lys607Glu
NM_001365048.1:c.1819A>G	NP_001351977.1:p.Lys607Glu
NM_001365049.1:c.1741A>G	NP_001351978.1:p.Lys581Glu
NM_015840.4:c.2626A>G	NP_056655.3:p.Lys876Glu
NM_015841.4:c.2569A>G	NP_056656.3:p.Lys857Glu
XM_006711113.2:c.1819A>G	XP_006711176.1:p.Lys607Glu
XM_011509061.2:c.1741A>G	XP_011507363.2:p.Lys581Glu
XM_024449674.1:c.2833A>G	XP_024305442.1:p.Lys945Glu