Canonical Allele Identifier: CA342634643

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557380C>A (hg19) ; chr1:g.154584904C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584904C>A , CM000663.2:g.154584904C>A	GRCh38
NC_000001.10:g.154557380C>A , CM000663.1:g.154557380C>A	GRCh37
NC_000001.9:g.152824004C>A	NCBI36
NG_011844.1:g.48058G>T
NG_011844.2:g.51657G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3477G>T	ENSP00000497790.2:n.3477G>T
ENST00000649724.2:c.3613G>T	ENSP00000497932.2:p.Ala1205Ser
ENST00000680270.2:c.3466G>T	ENSP00000505532.2:p.Ala1156Ser
ENST00000681056.2:c.3235G>T	ENSP00000506234.2:p.Ala1079Ser
ENST00000368471.8:c.2698G>T	ENSP00000357456.3:p.Ala900Ser
ENST00000368474.9:c.3583G>T MANE Select	ENSP00000357459.4:p.Ala1195Ser
ENST00000492630.2:n.2376G>T
ENST00000529168.2:c.3505G>T	ENSP00000431794.2:p.Ala1169Ser
ENST00000647682.2:n.3568G>T
ENST00000648231.2:c.2698G>T	ENSP00000497555.1:p.Ala900Ser
ENST00000648311.1:c.2698G>T	ENSP00000498137.1:p.Ala900Ser
ENST00000648714.2:c.*1058G>T	ENSP00000497434.2:n.*1058G>T
ENST00000649021.1:n.4319G>T
ENST00000649022.2:c.2698G>T	ENSP00000496896.2:p.Ala900Ser
ENST00000649042.1:c.2698G>T	ENSP00000497790.1:p.Ala900Ser
ENST00000649408.2:c.*749G>T	ENSP00000497386.2:n.*749G>T
ENST00000649724.1:c.2698G>T	ENSP00000497932.1:p.Ala900Ser
ENST00000649749.1:c.2698G>T	ENSP00000497210.1:p.Ala900Ser
ENST00000679375.1:c.*1815G>T	ENSP00000505887.1:n.*1815G>T
ENST00000679465.1:n.4444G>T
ENST00000679805.1:n.4319G>T
ENST00000679899.1:c.2641G>T	ENSP00000505996.1:p.Ala881Ser
ENST00000680270.1:c.2698G>T	ENSP00000505532.1:p.Ala900Ser
ENST00000680305.1:c.3400G>T	ENSP00000506312.1:p.Ala1134Ser
ENST00000681056.1:c.2698G>T	ENSP00000506234.1:p.Ala900Ser
ENST00000681235.1:c.*3105G>T	ENSP00000506606.1:n.*3105G>T
ENST00000681429.1:n.3251G>T
ENST00000681683.1:c.2698G>T	ENSP00000506666.1:p.Ala900Ser
ENST00000681786.1:n.4444G>T
ENST00000681901.1:c.*3183G>T	ENSP00000504883.1:n.*3183G>T
ENST00000368471.7:c.2698G>T	ENSP00000357456.3:p.Ala900Ser
ENST00000368474.8:c.3583G>T	ENSP00000357459.4:p.Ala1195Ser
ENST00000492630.1:n.342G>T
ENST00000529168.1:c.3490G>T	ENSP00000431794.1:p.Ala1164Ser
NM_001025107.2:c.2698G>T	NP_001020278.1:p.Ala900Ser
NM_001111.4:c.3583G>T	NP_001102.2:p.Ala1195Ser
NM_001193495.1:c.2698G>T	NP_001180424.1:p.Ala900Ser
NM_015840.3:c.3505G>T	NP_056655.2:p.Ala1169Ser
NM_015841.3:c.3448G>T	NP_056656.2:p.Ala1150Ser
XM_006711109.1:c.3613G>T	XP_006711172.1:p.Ala1205Ser
XM_006711111.2:c.2698G>T	XP_006711174.1:p.Ala900Ser
XM_006711112.1:c.2698G>T	XP_006711175.1:p.Ala900Ser
XM_006711113.1:c.2698G>T	XP_006711176.1:p.Ala900Ser
XM_011509060.1:c.3712G>T	XP_011507362.1:p.Ala1238Ser
XM_011509061.1:c.3634G>T	XP_011507363.1:p.Ala1212Ser
XM_011509062.1:c.3601G>T	XP_011507364.1:p.Ala1201Ser
NM_001025107.3:c.2698G>T	NP_001020278.1:p.Ala900Ser
NM_001111.5:c.3583G>T MANE Select	NP_001102.3:p.Ala1195Ser
NM_001193495.2:c.2698G>T	NP_001180424.1:p.Ala900Ser
NM_001365045.1:c.3610G>T	NP_001351974.1:p.Ala1204Ser
NM_001365046.1:c.2698G>T	NP_001351975.1:p.Ala900Ser
NM_001365047.1:c.2698G>T	NP_001351976.1:p.Ala900Ser
NM_001365048.1:c.2698G>T	NP_001351977.1:p.Ala900Ser
NM_001365049.1:c.2620G>T	NP_001351978.1:p.Ala874Ser
NM_015840.4:c.3505G>T	NP_056655.3:p.Ala1169Ser
NM_015841.4:c.3448G>T	NP_056656.3:p.Ala1150Ser
XM_006711113.2:c.2698G>T	XP_006711176.1:p.Ala900Ser
XM_011509061.2:c.2620G>T	XP_011507363.2:p.Ala874Ser
XM_024449674.1:c.3712G>T	XP_024305442.1:p.Ala1238Ser