Canonical Allele Identifier: CA342635983

Gene: ADAR

Linked Data

• dbSNP Id: rs1168323630
• gnomAD v2: 1-154560631-G-A
• MyVariant Identifiers: chr1:g.154560631G>A (hg19) ; chr1:g.154588155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588155G>A , CM000663.2:g.154588155G>A	GRCh38
NC_000001.10:g.154560631G>A , CM000663.1:g.154560631G>A	GRCh37
NC_000001.9:g.152827255G>A	NCBI36
NG_011844.1:g.44807C>T
NG_011844.2:g.48406C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.2883C>T	ENSP00000497790.2:n.2883C>T
ENST00000649724.2:c.3019C>T	ENSP00000497932.2:p.Gln1007Ter
ENST00000680270.2:c.2872C>T	ENSP00000505532.2:p.Gln958Ter
ENST00000681056.2:c.2641C>T	ENSP00000506234.2:p.Gln881Ter
ENST00000368471.8:c.2104C>T	ENSP00000357456.3:p.Gln702Ter
ENST00000368474.9:c.2989C>T MANE Select	ENSP00000357459.4:p.Gln997Ter
ENST00000529168.2:c.2911C>T	ENSP00000431794.2:p.Gln971Ter
ENST00000647682.2:n.2974C>T
ENST00000648231.2:c.2104C>T	ENSP00000497555.1:p.Gln702Ter
ENST00000648311.1:c.2104C>T	ENSP00000498137.1:p.Gln702Ter
ENST00000648714.2:c.*464C>T	ENSP00000497434.2:n.*464C>T
ENST00000649021.1:n.3317C>T
ENST00000649022.2:c.2104C>T	ENSP00000496896.2:p.Gln702Ter
ENST00000649042.1:c.2104C>T	ENSP00000497790.1:p.Gln702Ter
ENST00000649408.2:c.2989C>T	ENSP00000497386.2:p.Gln997Ter
ENST00000649724.1:c.2104C>T	ENSP00000497932.1:p.Gln702Ter
ENST00000649749.1:c.2104C>T	ENSP00000497210.1:p.Gln702Ter
ENST00000679375.1:c.*1221C>T	ENSP00000505887.1:n.*1221C>T
ENST00000679465.1:n.3442C>T
ENST00000679805.1:n.3317C>T
ENST00000679899.1:c.2047C>T	ENSP00000505996.1:p.Gln683Ter
ENST00000680270.1:c.2104C>T	ENSP00000505532.1:p.Gln702Ter
ENST00000680305.1:c.2989C>T	ENSP00000506312.1:p.Gln997Ter
ENST00000681056.1:c.2104C>T	ENSP00000506234.1:p.Gln702Ter
ENST00000681235.1:c.*2511C>T	ENSP00000506606.1:n.*2511C>T
ENST00000681429.1:n.2249C>T
ENST00000681683.1:c.2104C>T	ENSP00000506666.1:p.Gln702Ter
ENST00000681786.1:n.3442C>T
ENST00000681901.1:c.*2589C>T	ENSP00000504883.1:n.*2589C>T
ENST00000368471.7:c.2104C>T	ENSP00000357456.3:p.Gln702Ter
ENST00000368474.8:c.2989C>T	ENSP00000357459.4:p.Gln997Ter
ENST00000529168.1:c.2896C>T	ENSP00000431794.1:p.Gln966Ter
ENST00000530954.1:n.126C>T
ENST00000534279.1:n.448C>T
NM_001025107.2:c.2104C>T	NP_001020278.1:p.Gln702Ter
NM_001111.4:c.2989C>T	NP_001102.2:p.Gln997Ter
NM_001193495.1:c.2104C>T	NP_001180424.1:p.Gln702Ter
NM_015840.3:c.2911C>T	NP_056655.2:p.Gln971Ter
NM_015841.3:c.2854C>T	NP_056656.2:p.Gln952Ter
XM_006711109.1:c.3019C>T	XP_006711172.1:p.Gln1007Ter
XM_006711111.2:c.2104C>T	XP_006711174.1:p.Gln702Ter
XM_006711112.1:c.2104C>T	XP_006711175.1:p.Gln702Ter
XM_006711113.1:c.2104C>T	XP_006711176.1:p.Gln702Ter
XM_011509060.1:c.3118C>T	XP_011507362.1:p.Gln1040Ter
XM_011509061.1:c.3040C>T	XP_011507363.1:p.Gln1014Ter
XM_011509062.1:c.3007C>T	XP_011507364.1:p.Gln1003Ter
NM_001025107.3:c.2104C>T	NP_001020278.1:p.Gln702Ter
NM_001111.5:c.2989C>T MANE Select	NP_001102.3:p.Gln997Ter
NM_001193495.2:c.2104C>T	NP_001180424.1:p.Gln702Ter
NM_001365045.1:c.3016C>T	NP_001351974.1:p.Gln1006Ter
NM_001365046.1:c.2104C>T	NP_001351975.1:p.Gln702Ter
NM_001365047.1:c.2104C>T	NP_001351976.1:p.Gln702Ter
NM_001365048.1:c.2104C>T	NP_001351977.1:p.Gln702Ter
NM_001365049.1:c.2026C>T	NP_001351978.1:p.Gln676Ter
NM_015840.4:c.2911C>T	NP_056655.3:p.Gln971Ter
NM_015841.4:c.2854C>T	NP_056656.3:p.Gln952Ter
XM_006711113.2:c.2104C>T	XP_006711176.1:p.Gln702Ter
XM_011509061.2:c.2026C>T	XP_011507363.2:p.Gln676Ter
XM_024449674.1:c.3118C>T	XP_024305442.1:p.Gln1040Ter