Canonical Allele Identifier: CA10927925

Gene: ADAR

Linked Data

• ClinVar Variation Id: 1232134
• ClinVar RCV Id: RCV001612766
• dbSNP Id: rs1542796
• gnomAD v2: 1-154561661-C-G
• gnomAD v3: 1-154589185-C-G
• gnomAD v4: 1-154589185-C-G
• MyVariant Identifiers: chr1:g.154561661C>G (hg19) ; chr1:g.154589185C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589185C>G , CM000663.2:g.154589185C>G	GRCh38
NC_000001.10:g.154561661C>G , CM000663.1:g.154561661C>G	GRCh37
NC_000001.9:g.152828285C>G	NCBI36
NG_011844.1:g.43777G>C
NG_011844.2:g.47376G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2656+184G>C	ENSP00000497790.2:n.2656+184G>C
ENST00000649724.2:c.2792+184G>C	ENSP00000497932.2:n.2792+184G>C
ENST00000680270.2:c.2645+184G>C	ENSP00000505532.2:n.2645+184G>C
ENST00000681056.2:c.2414+184G>C	ENSP00000506234.2:n.2414+184G>C
ENST00000368471.8:c.1877+184G>C	ENSP00000357456.3:n.1877+184G>C
ENST00000368474.9:c.2762+184G>C MANE Select	ENSP00000357459.4:n.2762+184G>C
ENST00000529168.2:c.2684+184G>C	ENSP00000431794.2:n.2684+184G>C
ENST00000647682.2:n.2747+184G>C
ENST00000648231.2:c.1877+184G>C	ENSP00000497555.1:n.1877+184G>C
ENST00000648311.1:c.1877+184G>C	ENSP00000498137.1:n.1877+184G>C
ENST00000648714.2:c.*237+184G>C	ENSP00000497434.2:n.*237+184G>C
ENST00000649021.1:n.2798+184G>C
ENST00000649022.2:c.1877+184G>C	ENSP00000496896.2:n.1877+184G>C
ENST00000649042.1:c.1877+184G>C	ENSP00000497790.1:n.1877+184G>C
ENST00000649408.2:c.2762+184G>C	ENSP00000497386.2:n.2762+184G>C
ENST00000649724.1:c.1877+184G>C	ENSP00000497932.1:n.1877+184G>C
ENST00000649749.1:c.1877+184G>C	ENSP00000497210.1:n.1877+184G>C
ENST00000679375.1:c.*994+184G>C	ENSP00000505887.1:n.*994+184G>C
ENST00000679465.1:n.3215+184G>C
ENST00000679805.1:n.2798+184G>C
ENST00000679899.1:c.1820+184G>C	ENSP00000505996.1:n.1820+184G>C
ENST00000680270.1:c.1877+184G>C	ENSP00000505532.1:n.1877+184G>C
ENST00000680305.1:c.2762+184G>C	ENSP00000506312.1:n.2762+184G>C
ENST00000681056.1:c.1877+184G>C	ENSP00000506234.1:n.1877+184G>C
ENST00000681235.1:c.*2284+184G>C	ENSP00000506606.1:n.*2284+184G>C
ENST00000681429.1:n.2022+184G>C
ENST00000681683.1:c.1877+184G>C	ENSP00000506666.1:n.1877+184G>C
ENST00000681786.1:n.3215+184G>C
ENST00000681901.1:c.*2362+184G>C	ENSP00000504883.1:n.*2362+184G>C
ENST00000368471.7:c.1877+184G>C	ENSP00000357456.3:n.1877+184G>C
ENST00000368474.8:c.2762+184G>C	ENSP00000357459.4:n.2762+184G>C
ENST00000529168.1:c.2669+184G>C	ENSP00000431794.1:n.2669+184G>C
NM_001025107.2:c.1877+184G>C	NP_001020278.1:n.1877+184G>C
NM_001111.4:c.2762+184G>C	NP_001102.2:n.2762+184G>C
NM_001193495.1:c.1877+184G>C	NP_001180424.1:n.1877+184G>C
NM_015840.3:c.2684+184G>C	NP_056655.2:n.2684+184G>C
NM_015841.3:c.2627+184G>C	NP_056656.2:n.2627+184G>C
XM_006711109.1:c.2792+184G>C	XP_006711172.1:n.2792+184G>C
XM_006711111.2:c.1877+184G>C	XP_006711174.1:n.1877+184G>C
XM_006711112.1:c.1877+184G>C	XP_006711175.1:n.1877+184G>C
XM_006711113.1:c.1877+184G>C	XP_006711176.1:n.1877+184G>C
XM_011509060.1:c.2891+184G>C	XP_011507362.1:n.2891+184G>C
XM_011509061.1:c.2813+184G>C	XP_011507363.1:n.2813+184G>C
XM_011509062.1:c.2780+184G>C	XP_011507364.1:n.2780+184G>C
NM_001025107.3:c.1877+184G>C	NP_001020278.1:n.1877+184G>C
NM_001111.5:c.2762+184G>C MANE Select	NP_001102.3:n.2762+184G>C
NM_001193495.2:c.1877+184G>C	NP_001180424.1:n.1877+184G>C
NM_001365045.1:c.2789+184G>C	NP_001351974.1:n.2789+184G>C
NM_001365046.1:c.1877+184G>C	NP_001351975.1:n.1877+184G>C
NM_001365047.1:c.1877+184G>C	NP_001351976.1:n.1877+184G>C
NM_001365048.1:c.1877+184G>C	NP_001351977.1:n.1877+184G>C
NM_001365049.1:c.1799+184G>C	NP_001351978.1:n.1799+184G>C
NM_015840.4:c.2684+184G>C	NP_056655.3:n.2684+184G>C
NM_015841.4:c.2627+184G>C	NP_056656.3:n.2627+184G>C
XM_006711113.2:c.1877+184G>C	XP_006711176.1:n.1877+184G>C
XM_011509061.2:c.1799+184G>C	XP_011507363.2:n.1799+184G>C
XM_024449674.1:c.2891+184G>C	XP_024305442.1:n.2891+184G>C