Canonical Allele Identifier: CA342635200

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557804A>C (hg19) ; chr1:g.154585328A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154585328A>C , CM000663.2:g.154585328A>C	GRCh38
NC_000001.10:g.154557804A>C , CM000663.1:g.154557804A>C	GRCh37
NC_000001.9:g.152824428A>C	NCBI36
NG_011844.1:g.47634T>G
NG_011844.2:g.51233T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3226T>G	ENSP00000497790.2:n.3226T>G
ENST00000649724.2:c.3362T>G	ENSP00000497932.2:p.Ile1121Arg
ENST00000680270.2:c.3215T>G	ENSP00000505532.2:p.Ile1072Arg
ENST00000681056.2:c.2984T>G	ENSP00000506234.2:p.Ile995Arg
ENST00000368471.8:c.2447T>G	ENSP00000357456.3:p.Ile816Arg
ENST00000368474.9:c.3332T>G MANE Select	ENSP00000357459.4:p.Ile1111Arg
ENST00000492630.2:n.2125T>G
ENST00000529168.2:c.3254T>G	ENSP00000431794.2:p.Ile1085Arg
ENST00000647682.2:n.3317T>G
ENST00000648231.2:c.2447T>G	ENSP00000497555.1:p.Ile816Arg
ENST00000648311.1:c.2447T>G	ENSP00000498137.1:p.Ile816Arg
ENST00000648714.2:c.*807T>G	ENSP00000497434.2:n.*807T>G
ENST00000649021.1:n.4068T>G
ENST00000649022.2:c.2447T>G	ENSP00000496896.2:p.Ile816Arg
ENST00000649042.1:c.2447T>G	ENSP00000497790.1:p.Ile816Arg
ENST00000649408.2:c.*498T>G	ENSP00000497386.2:n.*498T>G
ENST00000649724.1:c.2447T>G	ENSP00000497932.1:p.Ile816Arg
ENST00000649749.1:c.2447T>G	ENSP00000497210.1:p.Ile816Arg
ENST00000679375.1:c.*1564T>G	ENSP00000505887.1:n.*1564T>G
ENST00000679465.1:n.4193T>G
ENST00000679805.1:n.4068T>G
ENST00000679899.1:c.2390T>G	ENSP00000505996.1:p.Ile797Arg
ENST00000680270.1:c.2447T>G	ENSP00000505532.1:p.Ile816Arg
ENST00000680305.1:c.3149T>G	ENSP00000506312.1:p.Ile1050Arg
ENST00000681056.1:c.2447T>G	ENSP00000506234.1:p.Ile816Arg
ENST00000681235.1:c.*2854T>G	ENSP00000506606.1:n.*2854T>G
ENST00000681429.1:n.3000T>G
ENST00000681683.1:c.2447T>G	ENSP00000506666.1:p.Ile816Arg
ENST00000681786.1:n.4193T>G
ENST00000681901.1:c.*2932T>G	ENSP00000504883.1:n.*2932T>G
ENST00000368471.7:c.2447T>G	ENSP00000357456.3:p.Ile816Arg
ENST00000368474.8:c.3332T>G	ENSP00000357459.4:p.Ile1111Arg
ENST00000492630.1:n.91T>G
ENST00000529168.1:c.3239T>G	ENSP00000431794.1:p.Ile1080Arg
NM_001025107.2:c.2447T>G	NP_001020278.1:p.Ile816Arg
NM_001111.4:c.3332T>G	NP_001102.2:p.Ile1111Arg
NM_001193495.1:c.2447T>G	NP_001180424.1:p.Ile816Arg
NM_015840.3:c.3254T>G	NP_056655.2:p.Ile1085Arg
NM_015841.3:c.3197T>G	NP_056656.2:p.Ile1066Arg
XM_006711109.1:c.3362T>G	XP_006711172.1:p.Ile1121Arg
XM_006711111.2:c.2447T>G	XP_006711174.1:p.Ile816Arg
XM_006711112.1:c.2447T>G	XP_006711175.1:p.Ile816Arg
XM_006711113.1:c.2447T>G	XP_006711176.1:p.Ile816Arg
XM_011509060.1:c.3461T>G	XP_011507362.1:p.Ile1154Arg
XM_011509061.1:c.3383T>G	XP_011507363.1:p.Ile1128Arg
XM_011509062.1:c.3350T>G	XP_011507364.1:p.Ile1117Arg
NM_001025107.3:c.2447T>G	NP_001020278.1:p.Ile816Arg
NM_001111.5:c.3332T>G MANE Select	NP_001102.3:p.Ile1111Arg
NM_001193495.2:c.2447T>G	NP_001180424.1:p.Ile816Arg
NM_001365045.1:c.3359T>G	NP_001351974.1:p.Ile1120Arg
NM_001365046.1:c.2447T>G	NP_001351975.1:p.Ile816Arg
NM_001365047.1:c.2447T>G	NP_001351976.1:p.Ile816Arg
NM_001365048.1:c.2447T>G	NP_001351977.1:p.Ile816Arg
NM_001365049.1:c.2369T>G	NP_001351978.1:p.Ile790Arg
NM_015840.4:c.3254T>G	NP_056655.3:p.Ile1085Arg
NM_015841.4:c.3197T>G	NP_056656.3:p.Ile1066Arg
XM_006711113.2:c.2447T>G	XP_006711176.1:p.Ile816Arg
XM_011509061.2:c.2369T>G	XP_011507363.2:p.Ile790Arg
XM_024449674.1:c.3461T>G	XP_024305442.1:p.Ile1154Arg