Canonical Allele Identifier: CA2648179259

Gene: ADAR

Linked Data

• gnomAD v4: 1-154589588-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589589del , CM000663.2:g.154589589del	GRCh38
NC_000001.10:g.154562065del , CM000663.1:g.154562065del	GRCh37
NC_000001.9:g.152828689del	NCBI36
NG_011844.1:g.43373del
NG_011844.2:g.46972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2563-127del	ENSP00000497790.2:n.2563-127del
ENST00000649724.2:c.2699-127del	ENSP00000497932.2:n.2699-127del
ENST00000680270.2:c.2552-127del	ENSP00000505532.2:n.2552-127del
ENST00000681056.2:c.2321-127del	ENSP00000506234.2:n.2321-127del
ENST00000368471.8:c.1784-127del	ENSP00000357456.3:n.1784-127del
ENST00000368474.9:c.2669-127del MANE Select	ENSP00000357459.4:n.2669-127del
ENST00000529168.2:c.2591-127del	ENSP00000431794.2:n.2591-127del
ENST00000647682.2:n.2654-127del
ENST00000648231.2:c.1784-127del	ENSP00000497555.1:n.1784-127del
ENST00000648311.1:c.1784-127del	ENSP00000498137.1:n.1784-127del
ENST00000648714.2:c.*144-127del	ENSP00000497434.2:n.*144-127del
ENST00000649021.1:n.2705-127del
ENST00000649022.2:c.1784-127del	ENSP00000496896.2:n.1784-127del
ENST00000649042.1:c.1784-127del	ENSP00000497790.1:n.1784-127del
ENST00000649408.2:c.2669-127del	ENSP00000497386.2:n.2669-127del
ENST00000649724.1:c.1784-127del	ENSP00000497932.1:n.1784-127del
ENST00000649749.1:c.1784-127del	ENSP00000497210.1:n.1784-127del
ENST00000679375.1:c.*901-127del	ENSP00000505887.1:n.*901-127del
ENST00000679465.1:n.3122-127del
ENST00000679805.1:n.2705-127del
ENST00000679899.1:c.1727-127del	ENSP00000505996.1:n.1727-127del
ENST00000680270.1:c.1784-127del	ENSP00000505532.1:n.1784-127del
ENST00000680305.1:c.2669-127del	ENSP00000506312.1:n.2669-127del
ENST00000681056.1:c.1784-127del	ENSP00000506234.1:n.1784-127del
ENST00000681235.1:c.*2191-127del	ENSP00000506606.1:n.*2191-127del
ENST00000681429.1:n.1929-127del
ENST00000681683.1:c.1784-127del	ENSP00000506666.1:n.1784-127del
ENST00000681786.1:n.3122-127del
ENST00000681901.1:c.*2269-127del	ENSP00000504883.1:n.*2269-127del
ENST00000368471.7:c.1784-127del	ENSP00000357456.3:n.1784-127del
ENST00000368474.8:c.2669-127del	ENSP00000357459.4:n.2669-127del
ENST00000529168.1:c.2576-127del	ENSP00000431794.1:n.2576-127del
NM_001025107.2:c.1784-127del	NP_001020278.1:n.1784-127del
NM_001111.4:c.2669-127del	NP_001102.2:n.2669-127del
NM_001193495.1:c.1784-127del	NP_001180424.1:n.1784-127del
NM_015840.3:c.2591-127del	NP_056655.2:n.2591-127del
NM_015841.3:c.2534-127del	NP_056656.2:n.2534-127del
XM_006711109.1:c.2699-127del	XP_006711172.1:n.2699-127del
XM_006711111.2:c.1784-127del	XP_006711174.1:n.1784-127del
XM_006711112.1:c.1784-127del	XP_006711175.1:n.1784-127del
XM_006711113.1:c.1784-127del	XP_006711176.1:n.1784-127del
XM_011509060.1:c.2798-127del	XP_011507362.1:n.2798-127del
XM_011509061.1:c.2720-127del	XP_011507363.1:n.2720-127del
XM_011509062.1:c.2687-127del	XP_011507364.1:n.2687-127del
NM_001025107.3:c.1784-127del	NP_001020278.1:n.1784-127del
NM_001111.5:c.2669-127del MANE Select	NP_001102.3:n.2669-127del
NM_001193495.2:c.1784-127del	NP_001180424.1:n.1784-127del
NM_001365045.1:c.2696-127del	NP_001351974.1:n.2696-127del
NM_001365046.1:c.1784-127del	NP_001351975.1:n.1784-127del
NM_001365047.1:c.1784-127del	NP_001351976.1:n.1784-127del
NM_001365048.1:c.1784-127del	NP_001351977.1:n.1784-127del
NM_001365049.1:c.1706-127del	NP_001351978.1:n.1706-127del
NM_015840.4:c.2591-127del	NP_056655.3:n.2591-127del
NM_015841.4:c.2534-127del	NP_056656.3:n.2534-127del
XM_006711113.2:c.1784-127del	XP_006711176.1:n.1784-127del
XM_011509061.2:c.1706-127del	XP_011507363.2:n.1706-127del
XM_024449674.1:c.2798-127del	XP_024305442.1:n.2798-127del