Canonical Allele Identifier: CA342634635

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557376T>A (hg19) ; chr1:g.154584900T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584900T>A , CM000663.2:g.154584900T>A	GRCh38
NC_000001.10:g.154557376T>A , CM000663.1:g.154557376T>A	GRCh37
NC_000001.9:g.152824000T>A	NCBI36
NG_011844.1:g.48062A>T
NG_011844.2:g.51661A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3481A>T	ENSP00000497790.2:n.3481A>T
ENST00000649724.2:c.3617A>T	ENSP00000497932.2:p.Lys1206Met
ENST00000680270.2:c.3470A>T	ENSP00000505532.2:p.Lys1157Met
ENST00000681056.2:c.3239A>T	ENSP00000506234.2:p.Lys1080Met
ENST00000368471.8:c.2702A>T	ENSP00000357456.3:p.Lys901Met
ENST00000368474.9:c.3587A>T MANE Select	ENSP00000357459.4:p.Lys1196Met
ENST00000492630.2:n.2380A>T
ENST00000529168.2:c.3509A>T	ENSP00000431794.2:p.Lys1170Met
ENST00000647682.2:n.3572A>T
ENST00000648231.2:c.2702A>T	ENSP00000497555.1:p.Lys901Met
ENST00000648311.1:c.2702A>T	ENSP00000498137.1:p.Lys901Met
ENST00000648714.2:c.*1062A>T	ENSP00000497434.2:n.*1062A>T
ENST00000649021.1:n.4323A>T
ENST00000649022.2:c.2702A>T	ENSP00000496896.2:p.Lys901Met
ENST00000649042.1:c.2702A>T	ENSP00000497790.1:p.Lys901Met
ENST00000649408.2:c.*753A>T	ENSP00000497386.2:n.*753A>T
ENST00000649724.1:c.2702A>T	ENSP00000497932.1:p.Lys901Met
ENST00000649749.1:c.2702A>T	ENSP00000497210.1:p.Lys901Met
ENST00000679375.1:c.*1819A>T	ENSP00000505887.1:n.*1819A>T
ENST00000679465.1:n.4448A>T
ENST00000679805.1:n.4323A>T
ENST00000679899.1:c.2645A>T	ENSP00000505996.1:p.Lys882Met
ENST00000680270.1:c.2702A>T	ENSP00000505532.1:p.Lys901Met
ENST00000680305.1:c.3404A>T	ENSP00000506312.1:p.Lys1135Met
ENST00000681056.1:c.2702A>T	ENSP00000506234.1:p.Lys901Met
ENST00000681235.1:c.*3109A>T	ENSP00000506606.1:n.*3109A>T
ENST00000681429.1:n.3255A>T
ENST00000681683.1:c.2702A>T	ENSP00000506666.1:p.Lys901Met
ENST00000681786.1:n.4448A>T
ENST00000681901.1:c.*3187A>T	ENSP00000504883.1:n.*3187A>T
ENST00000368471.7:c.2702A>T	ENSP00000357456.3:p.Lys901Met
ENST00000368474.8:c.3587A>T	ENSP00000357459.4:p.Lys1196Met
ENST00000492630.1:n.346A>T
ENST00000529168.1:c.3494A>T	ENSP00000431794.1:p.Lys1165Met
NM_001025107.2:c.2702A>T	NP_001020278.1:p.Lys901Met
NM_001111.4:c.3587A>T	NP_001102.2:p.Lys1196Met
NM_001193495.1:c.2702A>T	NP_001180424.1:p.Lys901Met
NM_015840.3:c.3509A>T	NP_056655.2:p.Lys1170Met
NM_015841.3:c.3452A>T	NP_056656.2:p.Lys1151Met
XM_006711109.1:c.3617A>T	XP_006711172.1:p.Lys1206Met
XM_006711111.2:c.2702A>T	XP_006711174.1:p.Lys901Met
XM_006711112.1:c.2702A>T	XP_006711175.1:p.Lys901Met
XM_006711113.1:c.2702A>T	XP_006711176.1:p.Lys901Met
XM_011509060.1:c.3716A>T	XP_011507362.1:p.Lys1239Met
XM_011509061.1:c.3638A>T	XP_011507363.1:p.Lys1213Met
XM_011509062.1:c.3605A>T	XP_011507364.1:p.Lys1202Met
NM_001025107.3:c.2702A>T	NP_001020278.1:p.Lys901Met
NM_001111.5:c.3587A>T MANE Select	NP_001102.3:p.Lys1196Met
NM_001193495.2:c.2702A>T	NP_001180424.1:p.Lys901Met
NM_001365045.1:c.3614A>T	NP_001351974.1:p.Lys1205Met
NM_001365046.1:c.2702A>T	NP_001351975.1:p.Lys901Met
NM_001365047.1:c.2702A>T	NP_001351976.1:p.Lys901Met
NM_001365048.1:c.2702A>T	NP_001351977.1:p.Lys901Met
NM_001365049.1:c.2624A>T	NP_001351978.1:p.Lys875Met
NM_015840.4:c.3509A>T	NP_056655.3:p.Lys1170Met
NM_015841.4:c.3452A>T	NP_056656.3:p.Lys1151Met
XM_006711113.2:c.2702A>T	XP_006711176.1:p.Lys901Met
XM_011509061.2:c.2624A>T	XP_011507363.2:p.Lys875Met
XM_024449674.1:c.3716A>T	XP_024305442.1:p.Lys1239Met