Canonical Allele Identifier: CA342636782

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589777-A-G
• MyVariant Identifiers: chr1:g.154562253A>G (hg19) ; chr1:g.154589777A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589777A>G , CM000663.2:g.154589777A>G	GRCh38
NC_000001.10:g.154562253A>G , CM000663.1:g.154562253A>G	GRCh37
NC_000001.9:g.152828877A>G	NCBI36
NG_011844.1:g.43185T>C
NG_011844.2:g.46784T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2542T>C	ENSP00000497790.2:n.2542T>C
ENST00000649724.2:c.2678T>C	ENSP00000497932.2:p.Val893Ala
ENST00000680270.2:c.2531T>C	ENSP00000505532.2:p.Val844Ala
ENST00000681056.2:c.2300T>C	ENSP00000506234.2:p.Val767Ala
ENST00000368471.8:c.1763T>C	ENSP00000357456.3:p.Val588Ala
ENST00000368474.9:c.2648T>C MANE Select	ENSP00000357459.4:p.Val883Ala
ENST00000529168.2:c.2570T>C	ENSP00000431794.2:p.Val857Ala
ENST00000647682.2:n.2633T>C
ENST00000648231.2:c.1763T>C	ENSP00000497555.1:p.Val588Ala
ENST00000648311.1:c.1763T>C	ENSP00000498137.1:p.Val588Ala
ENST00000648714.2:c.*123T>C	ENSP00000497434.2:n.*123T>C
ENST00000649021.1:n.2684T>C
ENST00000649022.2:c.1763T>C	ENSP00000496896.2:p.Val588Ala
ENST00000649042.1:c.1763T>C	ENSP00000497790.1:p.Val588Ala
ENST00000649408.2:c.2648T>C	ENSP00000497386.2:p.Val883Ala
ENST00000649724.1:c.1763T>C	ENSP00000497932.1:p.Val588Ala
ENST00000649749.1:c.1763T>C	ENSP00000497210.1:p.Val588Ala
ENST00000679375.1:c.*880T>C	ENSP00000505887.1:n.*880T>C
ENST00000679465.1:n.3101T>C
ENST00000679805.1:n.2684T>C
ENST00000679899.1:c.1706T>C	ENSP00000505996.1:p.Val569Ala
ENST00000680270.1:c.1763T>C	ENSP00000505532.1:p.Val588Ala
ENST00000680305.1:c.2648T>C	ENSP00000506312.1:p.Val883Ala
ENST00000681056.1:c.1763T>C	ENSP00000506234.1:p.Val588Ala
ENST00000681235.1:c.*2170T>C	ENSP00000506606.1:n.*2170T>C
ENST00000681429.1:n.1908T>C
ENST00000681683.1:c.1763T>C	ENSP00000506666.1:p.Val588Ala
ENST00000681786.1:n.3101T>C
ENST00000681901.1:c.*2248T>C	ENSP00000504883.1:n.*2248T>C
ENST00000368471.7:c.1763T>C	ENSP00000357456.3:p.Val588Ala
ENST00000368474.8:c.2648T>C	ENSP00000357459.4:p.Val883Ala
ENST00000529168.1:c.2555T>C	ENSP00000431794.1:p.Val852Ala
NM_001025107.2:c.1763T>C	NP_001020278.1:p.Val588Ala
NM_001111.4:c.2648T>C	NP_001102.2:p.Val883Ala
NM_001193495.1:c.1763T>C	NP_001180424.1:p.Val588Ala
NM_015840.3:c.2570T>C	NP_056655.2:p.Val857Ala
NM_015841.3:c.2513T>C	NP_056656.2:p.Val838Ala
XM_006711109.1:c.2678T>C	XP_006711172.1:p.Val893Ala
XM_006711111.2:c.1763T>C	XP_006711174.1:p.Val588Ala
XM_006711112.1:c.1763T>C	XP_006711175.1:p.Val588Ala
XM_006711113.1:c.1763T>C	XP_006711176.1:p.Val588Ala
XM_011509060.1:c.2777T>C	XP_011507362.1:p.Val926Ala
XM_011509061.1:c.2699T>C	XP_011507363.1:p.Val900Ala
XM_011509062.1:c.2666T>C	XP_011507364.1:p.Val889Ala
NM_001025107.3:c.1763T>C	NP_001020278.1:p.Val588Ala
NM_001111.5:c.2648T>C MANE Select	NP_001102.3:p.Val883Ala
NM_001193495.2:c.1763T>C	NP_001180424.1:p.Val588Ala
NM_001365045.1:c.2675T>C	NP_001351974.1:p.Val892Ala
NM_001365046.1:c.1763T>C	NP_001351975.1:p.Val588Ala
NM_001365047.1:c.1763T>C	NP_001351976.1:p.Val588Ala
NM_001365048.1:c.1763T>C	NP_001351977.1:p.Val588Ala
NM_001365049.1:c.1685T>C	NP_001351978.1:p.Val562Ala
NM_015840.4:c.2570T>C	NP_056655.3:p.Val857Ala
NM_015841.4:c.2513T>C	NP_056656.3:p.Val838Ala
XM_006711113.2:c.1763T>C	XP_006711176.1:p.Val588Ala
XM_011509061.2:c.1685T>C	XP_011507363.2:p.Val562Ala
XM_024449674.1:c.2777T>C	XP_024305442.1:p.Val926Ala