Canonical Allele Identifier: CA342604662

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154574816C>T (hg19) ; chr1:g.154602340C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154602340C>T , CM000663.2:g.154602340C>T	GRCh38
NC_000001.10:g.154574816C>T , CM000663.1:g.154574816C>T	GRCh37
NC_000001.9:g.152841440C>T	NCBI36
NG_011844.1:g.30622G>A
NG_011844.2:g.34221G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.287+45G>A	ENSP00000497790.2:n.287+45G>A
ENST00000649724.2:c.332G>A	ENSP00000497932.2:p.Ser111Asn
ENST00000680270.2:c.332G>A	ENSP00000505532.2:p.Ser111Asn
ENST00000681056.2:c.46-92G>A	ENSP00000506234.2:n.46-92G>A
ENST00000368471.8:c.-584G>A	ENSP00000357456.3:n.-584G>A
ENST00000368474.9:c.302G>A MANE Select	ENSP00000357459.4:p.Ser101Asn
ENST00000471068.2:n.390+45G>A
ENST00000526905.2:n.257+45G>A
ENST00000529168.2:c.302G>A	ENSP00000431794.2:p.Ser101Asn
ENST00000647682.2:n.124-92G>A
ENST00000648231.2:c.-584G>A	ENSP00000497555.1:n.-584G>A
ENST00000648311.1:c.-584G>A	ENSP00000498137.1:n.-584G>A
ENST00000648714.2:c.302G>A	ENSP00000497434.2:p.Ser101Asn
ENST00000648871.1:c.-492-92G>A	ENSP00000497793.1:n.-492-92G>A
ENST00000649021.1:n.338G>A
ENST00000649022.2:c.-584G>A	ENSP00000496896.2:n.-584G>A
ENST00000649042.1:c.-493+45G>A	ENSP00000497790.1:n.-493+45G>A
ENST00000649408.2:c.302G>A	ENSP00000497386.2:p.Ser101Asn
ENST00000649724.1:c.-584G>A	ENSP00000497932.1:n.-584G>A
ENST00000649749.1:c.-584G>A	ENSP00000497210.1:n.-584G>A
ENST00000679375.1:c.-492-92G>A	ENSP00000505887.1:n.-492-92G>A
ENST00000679465.1:n.500G>A
ENST00000679805.1:n.338G>A
ENST00000679899.1:c.-584G>A	ENSP00000505996.1:n.-584G>A
ENST00000680270.1:c.-437G>A	ENSP00000505532.1:n.-437G>A
ENST00000680305.1:c.302G>A	ENSP00000506312.1:p.Ser101Asn
ENST00000680472.1:n.341G>A
ENST00000681056.1:c.-492-92G>A	ENSP00000506234.1:n.-492-92G>A
ENST00000681235.1:c.257+45G>A	ENSP00000506606.1:n.257+45G>A
ENST00000681683.1:c.-493+45G>A	ENSP00000506666.1:n.-493+45G>A
ENST00000681786.1:n.500G>A
ENST00000681901.1:c.257+45G>A	ENSP00000504883.1:n.257+45G>A
ENST00000368471.7:c.-584G>A	ENSP00000357456.3:n.-584G>A
ENST00000368474.8:c.302G>A	ENSP00000357459.4:p.Ser101Asn
ENST00000463920.5:n.275+45G>A
ENST00000471068.1:n.333G>A
ENST00000494866.1:n.300+45G>A
ENST00000526905.1:n.349G>A
ENST00000529168.1:c.287G>A	ENSP00000431794.1:p.Ser96Asn
NM_001025107.2:c.-584G>A	NP_001020278.1:n.-584G>A
NM_001111.4:c.302G>A	NP_001102.2:p.Ser101Asn
NM_001193495.1:c.-584G>A	NP_001180424.1:n.-584G>A
NM_015840.3:c.302G>A	NP_056655.2:p.Ser101Asn
NM_015841.3:c.302G>A	NP_056656.2:p.Ser101Asn
XM_006711109.1:c.332G>A	XP_006711172.1:p.Ser111Asn
XM_006711111.2:c.-493+45G>A	XP_006711174.1:n.-493+45G>A
XM_006711112.1:c.-493+45G>A	XP_006711175.1:n.-493+45G>A
XM_006711113.1:c.-493+45G>A	XP_006711176.1:n.-493+45G>A
XM_011509060.1:c.431G>A	XP_011507362.1:p.Ser144Asn
XM_011509061.1:c.431G>A	XP_011507363.1:p.Ser144Asn
XM_011509062.1:c.320G>A	XP_011507364.1:p.Ser107Asn
NM_001025107.3:c.-584G>A	NP_001020278.1:n.-584G>A
NM_001111.5:c.302G>A MANE Select	NP_001102.3:p.Ser101Asn
NM_001193495.2:c.-584G>A	NP_001180424.1:n.-584G>A
NM_001365045.1:c.329G>A	NP_001351974.1:p.Ser110Asn
NM_001365046.1:c.-493+45G>A	NP_001351975.1:n.-493+45G>A
NM_001365047.1:c.-493+45G>A	NP_001351976.1:n.-493+45G>A
NM_001365048.1:c.-584G>A	NP_001351977.1:n.-584G>A
NM_001365049.1:c.-493+45G>A	NP_001351978.1:n.-493+45G>A
NM_015840.4:c.302G>A	NP_056655.3:p.Ser101Asn
NM_015841.4:c.302G>A	NP_056656.3:p.Ser101Asn
XM_006711113.2:c.-493+45G>A	XP_006711176.1:n.-493+45G>A
XM_011509061.2:c.-584G>A	XP_011507363.2:n.-584G>A
XM_024449674.1:c.431G>A	XP_024305442.1:p.Ser144Asn