Canonical Allele Identifier: CA342636717

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589457-G-T
• MyVariant Identifiers: chr1:g.154561933G>T (hg19) ; chr1:g.154589457G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589457G>T , CM000663.2:g.154589457G>T	GRCh38
NC_000001.10:g.154561933G>T , CM000663.1:g.154561933G>T	GRCh37
NC_000001.9:g.152828557G>T	NCBI36
NG_011844.1:g.43505C>A
NG_011844.2:g.47104C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.2568C>A	ENSP00000497790.2:n.2568C>A
ENST00000649724.2:c.2704C>A	ENSP00000497932.2:p.Arg902Ser
ENST00000680270.2:c.2557C>A	ENSP00000505532.2:p.Arg853Ser
ENST00000681056.2:c.2326C>A	ENSP00000506234.2:p.Arg776Ser
ENST00000368471.8:c.1789C>A	ENSP00000357456.3:p.Arg597Ser
ENST00000368474.9:c.2674C>A MANE Select	ENSP00000357459.4:p.Arg892Ser
ENST00000529168.2:c.2596C>A	ENSP00000431794.2:p.Arg866Ser
ENST00000647682.2:n.2659C>A
ENST00000648231.2:c.1789C>A	ENSP00000497555.1:p.Arg597Ser
ENST00000648311.1:c.1789C>A	ENSP00000498137.1:p.Arg597Ser
ENST00000648714.2:c.*149C>A	ENSP00000497434.2:n.*149C>A
ENST00000649021.1:n.2710C>A
ENST00000649022.2:c.1789C>A	ENSP00000496896.2:p.Arg597Ser
ENST00000649042.1:c.1789C>A	ENSP00000497790.1:p.Arg597Ser
ENST00000649408.2:c.2674C>A	ENSP00000497386.2:p.Arg892Ser
ENST00000649724.1:c.1789C>A	ENSP00000497932.1:p.Arg597Ser
ENST00000649749.1:c.1789C>A	ENSP00000497210.1:p.Arg597Ser
ENST00000679375.1:c.*906C>A	ENSP00000505887.1:n.*906C>A
ENST00000679465.1:n.3127C>A
ENST00000679805.1:n.2710C>A
ENST00000679899.1:c.1732C>A	ENSP00000505996.1:p.Arg578Ser
ENST00000680270.1:c.1789C>A	ENSP00000505532.1:p.Arg597Ser
ENST00000680305.1:c.2674C>A	ENSP00000506312.1:p.Arg892Ser
ENST00000681056.1:c.1789C>A	ENSP00000506234.1:p.Arg597Ser
ENST00000681235.1:c.*2196C>A	ENSP00000506606.1:n.*2196C>A
ENST00000681429.1:n.1934C>A
ENST00000681683.1:c.1789C>A	ENSP00000506666.1:p.Arg597Ser
ENST00000681786.1:n.3127C>A
ENST00000681901.1:c.*2274C>A	ENSP00000504883.1:n.*2274C>A
ENST00000368471.7:c.1789C>A	ENSP00000357456.3:p.Arg597Ser
ENST00000368474.8:c.2674C>A	ENSP00000357459.4:p.Arg892Ser
ENST00000529168.1:c.2581C>A	ENSP00000431794.1:p.Arg861Ser
NM_001025107.2:c.1789C>A	NP_001020278.1:p.Arg597Ser
NM_001111.4:c.2674C>A	NP_001102.2:p.Arg892Ser
NM_001193495.1:c.1789C>A	NP_001180424.1:p.Arg597Ser
NM_015840.3:c.2596C>A	NP_056655.2:p.Arg866Ser
NM_015841.3:c.2539C>A	NP_056656.2:p.Arg847Ser
XM_006711109.1:c.2704C>A	XP_006711172.1:p.Arg902Ser
XM_006711111.2:c.1789C>A	XP_006711174.1:p.Arg597Ser
XM_006711112.1:c.1789C>A	XP_006711175.1:p.Arg597Ser
XM_006711113.1:c.1789C>A	XP_006711176.1:p.Arg597Ser
XM_011509060.1:c.2803C>A	XP_011507362.1:p.Arg935Ser
XM_011509061.1:c.2725C>A	XP_011507363.1:p.Arg909Ser
XM_011509062.1:c.2692C>A	XP_011507364.1:p.Arg898Ser
NM_001025107.3:c.1789C>A	NP_001020278.1:p.Arg597Ser
NM_001111.5:c.2674C>A MANE Select	NP_001102.3:p.Arg892Ser
NM_001193495.2:c.1789C>A	NP_001180424.1:p.Arg597Ser
NM_001365045.1:c.2701C>A	NP_001351974.1:p.Arg901Ser
NM_001365046.1:c.1789C>A	NP_001351975.1:p.Arg597Ser
NM_001365047.1:c.1789C>A	NP_001351976.1:p.Arg597Ser
NM_001365048.1:c.1789C>A	NP_001351977.1:p.Arg597Ser
NM_001365049.1:c.1711C>A	NP_001351978.1:p.Arg571Ser
NM_015840.4:c.2596C>A	NP_056655.3:p.Arg866Ser
NM_015841.4:c.2539C>A	NP_056656.3:p.Arg847Ser
XM_006711113.2:c.1789C>A	XP_006711176.1:p.Arg597Ser
XM_011509061.2:c.1711C>A	XP_011507363.2:p.Arg571Ser
XM_024449674.1:c.2803C>A	XP_024305442.1:p.Arg935Ser