Canonical Allele Identifier: CA1007923698

Gene: ADAR

Linked Data

• dbSNP Id: rs1697006704
• gnomAD v3: 1-154589790-CAG-C
• gnomAD v4: 1-154589790-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589793_154589794del , CM000663.2:g.154589793_154589794del	GRCh38
NC_000001.10:g.154562269_154562270del , CM000663.1:g.154562269_154562270del	GRCh37
NC_000001.9:g.152828893_152828894del	NCBI36
NG_011844.1:g.43170_43171del
NG_011844.2:g.46769_46770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2527_2528del	ENSP00000497790.2:n.2527_2528del
ENST00000649724.2:c.2663_2664del	ENSP00000497932.2:p.Ser888Ter
ENST00000680270.2:c.2516_2517del	ENSP00000505532.2:p.Ser839Ter
ENST00000681056.2:c.2285_2286del	ENSP00000506234.2:p.Ser762Ter
ENST00000368471.8:c.1748_1749del	ENSP00000357456.3:p.Ser583Ter
ENST00000368474.9:c.2633_2634del MANE Select	ENSP00000357459.4:p.Ser878Ter
ENST00000529168.2:c.2555_2556del	ENSP00000431794.2:p.Ser852Ter
ENST00000647682.2:n.2618_2619del
ENST00000648231.2:c.1748_1749del	ENSP00000497555.1:p.Ser583Ter
ENST00000648311.1:c.1748_1749del	ENSP00000498137.1:p.Ser583Ter
ENST00000648714.2:c.*108_*109del	ENSP00000497434.2:n.*108_*109del
ENST00000649021.1:n.2669_2670del
ENST00000649022.2:c.1748_1749del	ENSP00000496896.2:p.Ser583Ter
ENST00000649042.1:c.1748_1749del	ENSP00000497790.1:p.Ser583Ter
ENST00000649408.2:c.2633_2634del	ENSP00000497386.2:p.Ser878Ter
ENST00000649724.1:c.1748_1749del	ENSP00000497932.1:p.Ser583Ter
ENST00000649749.1:c.1748_1749del	ENSP00000497210.1:p.Ser583Ter
ENST00000679375.1:c.*865_*866del	ENSP00000505887.1:n.*865_*866del
ENST00000679465.1:n.3086_3087del
ENST00000679805.1:n.2669_2670del
ENST00000679899.1:c.1691_1692del	ENSP00000505996.1:p.Ser564Ter
ENST00000680270.1:c.1748_1749del	ENSP00000505532.1:p.Ser583Ter
ENST00000680305.1:c.2633_2634del	ENSP00000506312.1:p.Ser878Ter
ENST00000681056.1:c.1748_1749del	ENSP00000506234.1:p.Ser583Ter
ENST00000681235.1:c.*2155_*2156del	ENSP00000506606.1:n.*2155_*2156del
ENST00000681429.1:n.1893_1894del
ENST00000681683.1:c.1748_1749del	ENSP00000506666.1:p.Ser583Ter
ENST00000681786.1:n.3086_3087del
ENST00000681901.1:c.*2233_*2234del	ENSP00000504883.1:n.*2233_*2234del
ENST00000368471.7:c.1748_1749del	ENSP00000357456.3:p.Ser583Ter
ENST00000368474.8:c.2633_2634del	ENSP00000357459.4:p.Ser878Ter
ENST00000529168.1:c.2540_2541del	ENSP00000431794.1:p.Ser847Ter
NM_001025107.2:c.1748_1749del	NP_001020278.1:p.Ser583Ter
NM_001111.4:c.2633_2634del	NP_001102.2:p.Ser878Ter
NM_001193495.1:c.1748_1749del	NP_001180424.1:p.Ser583Ter
NM_015840.3:c.2555_2556del	NP_056655.2:p.Ser852Ter
NM_015841.3:c.2498_2499del	NP_056656.2:p.Ser833Ter
XM_006711109.1:c.2663_2664del	XP_006711172.1:p.Ser888Ter
XM_006711111.2:c.1748_1749del	XP_006711174.1:p.Ser583Ter
XM_006711112.1:c.1748_1749del	XP_006711175.1:p.Ser583Ter
XM_006711113.1:c.1748_1749del	XP_006711176.1:p.Ser583Ter
XM_011509060.1:c.2762_2763del	XP_011507362.1:p.Ser921Ter
XM_011509061.1:c.2684_2685del	XP_011507363.1:p.Ser895Ter
XM_011509062.1:c.2651_2652del	XP_011507364.1:p.Ser884Ter
NM_001025107.3:c.1748_1749del	NP_001020278.1:p.Ser583Ter
NM_001111.5:c.2633_2634del MANE Select	NP_001102.3:p.Ser878Ter
NM_001193495.2:c.1748_1749del	NP_001180424.1:p.Ser583Ter
NM_001365045.1:c.2660_2661del	NP_001351974.1:p.Ser887Ter
NM_001365046.1:c.1748_1749del	NP_001351975.1:p.Ser583Ter
NM_001365047.1:c.1748_1749del	NP_001351976.1:p.Ser583Ter
NM_001365048.1:c.1748_1749del	NP_001351977.1:p.Ser583Ter
NM_001365049.1:c.1670_1671del	NP_001351978.1:p.Ser557Ter
NM_015840.4:c.2555_2556del	NP_056655.3:p.Ser852Ter
NM_015841.4:c.2498_2499del	NP_056656.3:p.Ser833Ter
XM_006711113.2:c.1748_1749del	XP_006711176.1:p.Ser583Ter
XM_011509061.2:c.1670_1671del	XP_011507363.2:p.Ser557Ter
XM_024449674.1:c.2762_2763del	XP_024305442.1:p.Ser921Ter