Canonical Allele Identifier: CA1131671

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602027G>T , CM000663.2:g.154602027G>T	GRCh38
NC_000001.10:g.154574503G>T , CM000663.1:g.154574503G>T	GRCh37
NC_000001.9:g.152841127G>T	NCBI36
NG_011844.1:g.30935C>A
NG_011844.2:g.34534C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.509C>A	ENSP00000497790.2:n.509C>A
ENST00000649724.2:c.645C>A	ENSP00000497932.2:p.Asn215Lys
ENST00000680270.2:c.636+9C>A	ENSP00000505532.2:n.636+9C>A
ENST00000681056.2:c.267C>A	ENSP00000506234.2:p.Asn89Lys
ENST00000368471.8:c.-271C>A	ENSP00000357456.3:n.-271C>A
ENST00000368474.9:c.615C>A MANE Select	ENSP00000357459.4:p.Asn205Lys
ENST00000529168.2:c.615C>A	ENSP00000431794.2:p.Asn205Lys
ENST00000647682.2:n.345C>A
ENST00000648231.2:c.-271C>A	ENSP00000497555.1:n.-271C>A
ENST00000648311.1:c.-271C>A	ENSP00000498137.1:n.-271C>A
ENST00000648714.2:c.615C>A	ENSP00000497434.2:p.Asn205Lys
ENST00000648871.1:c.-271C>A	ENSP00000497793.1:n.-271C>A
ENST00000649021.1:n.651C>A
ENST00000649022.2:c.-271C>A	ENSP00000496896.2:n.-271C>A
ENST00000649042.1:c.-271C>A	ENSP00000497790.1:n.-271C>A
ENST00000649408.2:c.615C>A	ENSP00000497386.2:p.Asn205Lys
ENST00000649724.1:c.-271C>A	ENSP00000497932.1:n.-271C>A
ENST00000649749.1:c.-271C>A	ENSP00000497210.1:n.-271C>A
ENST00000679375.1:c.-271C>A	ENSP00000505887.1:n.-271C>A
ENST00000679465.1:n.813C>A
ENST00000679805.1:n.651C>A
ENST00000679899.1:c.-271C>A	ENSP00000505996.1:n.-271C>A
ENST00000680270.1:c.-133+9C>A	ENSP00000505532.1:n.-133+9C>A
ENST00000680305.1:c.615C>A	ENSP00000506312.1:p.Asn205Lys
ENST00000680472.1:n.654C>A
ENST00000681056.1:c.-271C>A	ENSP00000506234.1:n.-271C>A
ENST00000681235.1:c.*215C>A	ENSP00000506606.1:n.*215C>A
ENST00000681683.1:c.-271C>A	ENSP00000506666.1:n.-271C>A
ENST00000681786.1:n.813C>A
ENST00000681901.1:c.*215C>A	ENSP00000504883.1:n.*215C>A
ENST00000368471.7:c.-271C>A	ENSP00000357456.3:n.-271C>A
ENST00000368474.8:c.615C>A	ENSP00000357459.4:p.Asn205Lys
ENST00000463920.5:n.497C>A
ENST00000529168.1:c.600C>A	ENSP00000431794.1:p.Asn200Lys
NM_001025107.2:c.-271C>A	NP_001020278.1:n.-271C>A
NM_001111.4:c.615C>A	NP_001102.2:p.Asn205Lys
NM_001193495.1:c.-271C>A	NP_001180424.1:n.-271C>A
NM_015840.3:c.615C>A	NP_056655.2:p.Asn205Lys
NM_015841.3:c.615C>A	NP_056656.2:p.Asn205Lys
XM_006711109.1:c.645C>A	XP_006711172.1:p.Asn215Lys
XM_006711111.2:c.-271C>A	XP_006711174.1:n.-271C>A
XM_006711112.1:c.-271C>A	XP_006711175.1:n.-271C>A
XM_006711113.1:c.-271C>A	XP_006711176.1:n.-271C>A
XM_011509060.1:c.744C>A	XP_011507362.1:p.Asn248Lys
XM_011509061.1:c.744C>A	XP_011507363.1:p.Asn248Lys
XM_011509062.1:c.633C>A	XP_011507364.1:p.Asn211Lys
NM_001025107.3:c.-271C>A	NP_001020278.1:n.-271C>A
NM_001111.5:c.615C>A MANE Select	NP_001102.3:p.Asn205Lys
NM_001193495.2:c.-271C>A	NP_001180424.1:n.-271C>A
NM_001365045.1:c.642C>A	NP_001351974.1:p.Asn214Lys
NM_001365046.1:c.-271C>A	NP_001351975.1:n.-271C>A
NM_001365047.1:c.-271C>A	NP_001351976.1:n.-271C>A
NM_001365048.1:c.-271C>A	NP_001351977.1:n.-271C>A
NM_001365049.1:c.-271C>A	NP_001351978.1:n.-271C>A
NM_015840.4:c.615C>A	NP_056655.3:p.Asn205Lys
NM_015841.4:c.615C>A	NP_056656.3:p.Asn205Lys
XM_006711113.2:c.-271C>A	XP_006711176.1:n.-271C>A
XM_011509061.2:c.-271C>A	XP_011507363.2:n.-271C>A
XM_024449674.1:c.744C>A	XP_024305442.1:p.Asn248Lys