Canonical Allele Identifier: CA2573911944

Gene: ADAR

Linked Data

• gnomAD v4: 1-154584769-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584769G>A , CM000663.2:g.154584769G>A	GRCh38
NC_000001.10:g.154557245G>A , CM000663.1:g.154557245G>A	GRCh37
NC_000001.9:g.152823869G>A	NCBI36
NG_011844.1:g.48193C>T
NG_011844.2:g.51792C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3612C>T	ENSP00000497790.2:n.3612C>T
ENST00000649724.2:c.*37C>T	ENSP00000497932.2:n.*37C>T
ENST00000680270.2:c.3601C>T	ENSP00000505532.2:n.3601C>T
ENST00000681056.2:c.*37C>T	ENSP00000506234.2:n.*37C>T
ENST00000368471.8:c.*37C>T	ENSP00000357456.3:n.*37C>T
ENST00000368474.9:c.*37C>T MANE Select	ENSP00000357459.4:n.*37C>T
ENST00000492630.2:n.2511C>T
ENST00000529168.2:c.*37C>T	ENSP00000431794.2:n.*37C>T
ENST00000647682.2:n.3703C>T
ENST00000648231.2:c.*37C>T	ENSP00000497555.1:n.*37C>T
ENST00000648311.1:c.*37C>T	ENSP00000498137.1:n.*37C>T
ENST00000648714.2:c.*1193C>T	ENSP00000497434.2:n.*1193C>T
ENST00000649021.1:n.4454C>T
ENST00000649022.2:c.*37C>T	ENSP00000496896.2:n.*37C>T
ENST00000649042.1:c.*37C>T	ENSP00000497790.1:n.*37C>T
ENST00000649408.2:c.*884C>T	ENSP00000497386.2:n.*884C>T
ENST00000649724.1:c.*37C>T	ENSP00000497932.1:n.*37C>T
ENST00000649749.1:c.*37C>T	ENSP00000497210.1:n.*37C>T
ENST00000679375.1:c.*1950C>T	ENSP00000505887.1:n.*1950C>T
ENST00000679465.1:n.4579C>T
ENST00000679805.1:n.4454C>T
ENST00000679899.1:c.*37C>T	ENSP00000505996.1:n.*37C>T
ENST00000680270.1:c.*37C>T	ENSP00000505532.1:n.*37C>T
ENST00000680305.1:c.*37C>T	ENSP00000506312.1:n.*37C>T
ENST00000681056.1:c.*37C>T	ENSP00000506234.1:n.*37C>T
ENST00000681235.1:c.*3240C>T	ENSP00000506606.1:n.*3240C>T
ENST00000681429.1:n.3386C>T
ENST00000681683.1:c.*37C>T	ENSP00000506666.1:n.*37C>T
ENST00000681786.1:n.4579C>T
ENST00000681901.1:c.*3318C>T	ENSP00000504883.1:n.*3318C>T
ENST00000368471.7:c.*37C>T	ENSP00000357456.3:n.*37C>T
ENST00000368474.8:c.*37C>T	ENSP00000357459.4:n.*37C>T
ENST00000492630.1:n.477C>T
NM_001025107.2:c.*37C>T	NP_001020278.1:n.*37C>T
NM_001111.4:c.*37C>T	NP_001102.2:n.*37C>T
NM_001193495.1:c.*37C>T	NP_001180424.1:n.*37C>T
NM_015840.3:c.*37C>T	NP_056655.2:n.*37C>T
NM_015841.3:c.*37C>T	NP_056656.2:n.*37C>T
XM_006711109.1:c.*37C>T	XP_006711172.1:n.*37C>T
XM_006711111.2:c.*37C>T	XP_006711174.1:n.*37C>T
XM_006711112.1:c.*37C>T	XP_006711175.1:n.*37C>T
XM_006711113.1:c.*37C>T	XP_006711176.1:n.*37C>T
XM_011509060.1:c.*37C>T	XP_011507362.1:n.*37C>T
XM_011509061.1:c.*37C>T	XP_011507363.1:n.*37C>T
XM_011509062.1:c.*37C>T	XP_011507364.1:n.*37C>T
NM_001025107.3:c.*37C>T	NP_001020278.1:n.*37C>T
NM_001111.5:c.*37C>T MANE Select	NP_001102.3:n.*37C>T
NM_001193495.2:c.*37C>T	NP_001180424.1:n.*37C>T
NM_001365045.1:c.*37C>T	NP_001351974.1:n.*37C>T
NM_001365046.1:c.*37C>T	NP_001351975.1:n.*37C>T
NM_001365047.1:c.*37C>T	NP_001351976.1:n.*37C>T
NM_001365048.1:c.*37C>T	NP_001351977.1:n.*37C>T
NM_001365049.1:c.*37C>T	NP_001351978.1:n.*37C>T
NM_015840.4:c.*37C>T	NP_056655.3:n.*37C>T
NM_015841.4:c.*37C>T	NP_056656.3:n.*37C>T
XM_006711113.2:c.*37C>T	XP_006711176.1:n.*37C>T
XM_011509061.2:c.*37C>T	XP_011507363.2:n.*37C>T
XM_024449674.1:c.*37C>T	XP_024305442.1:n.*37C>T