Canonical Allele Identifier: CA342636598

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154561881C>T (hg19) ; chr1:g.154589405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589405C>T , CM000663.2:g.154589405C>T	GRCh38
NC_000001.10:g.154561881C>T , CM000663.1:g.154561881C>T	GRCh37
NC_000001.9:g.152828505C>T	NCBI36
NG_011844.1:g.43557G>A
NG_011844.2:g.47156G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2620G>A	ENSP00000497790.2:n.2620G>A
ENST00000649724.2:c.2756G>A	ENSP00000497932.2:p.Cys919Tyr
ENST00000680270.2:c.2609G>A	ENSP00000505532.2:p.Cys870Tyr
ENST00000681056.2:c.2378G>A	ENSP00000506234.2:p.Cys793Tyr
ENST00000368471.8:c.1841G>A	ENSP00000357456.3:p.Cys614Tyr
ENST00000368474.9:c.2726G>A MANE Select	ENSP00000357459.4:p.Cys909Tyr
ENST00000529168.2:c.2648G>A	ENSP00000431794.2:p.Cys883Tyr
ENST00000647682.2:n.2711G>A
ENST00000648231.2:c.1841G>A	ENSP00000497555.1:p.Cys614Tyr
ENST00000648311.1:c.1841G>A	ENSP00000498137.1:p.Cys614Tyr
ENST00000648714.2:c.*201G>A	ENSP00000497434.2:n.*201G>A
ENST00000649021.1:n.2762G>A
ENST00000649022.2:c.1841G>A	ENSP00000496896.2:p.Cys614Tyr
ENST00000649042.1:c.1841G>A	ENSP00000497790.1:p.Cys614Tyr
ENST00000649408.2:c.2726G>A	ENSP00000497386.2:p.Cys909Tyr
ENST00000649724.1:c.1841G>A	ENSP00000497932.1:p.Cys614Tyr
ENST00000649749.1:c.1841G>A	ENSP00000497210.1:p.Cys614Tyr
ENST00000679375.1:c.*958G>A	ENSP00000505887.1:n.*958G>A
ENST00000679465.1:n.3179G>A
ENST00000679805.1:n.2762G>A
ENST00000679899.1:c.1784G>A	ENSP00000505996.1:p.Cys595Tyr
ENST00000680270.1:c.1841G>A	ENSP00000505532.1:p.Cys614Tyr
ENST00000680305.1:c.2726G>A	ENSP00000506312.1:p.Cys909Tyr
ENST00000681056.1:c.1841G>A	ENSP00000506234.1:p.Cys614Tyr
ENST00000681235.1:c.*2248G>A	ENSP00000506606.1:n.*2248G>A
ENST00000681429.1:n.1986G>A
ENST00000681683.1:c.1841G>A	ENSP00000506666.1:p.Cys614Tyr
ENST00000681786.1:n.3179G>A
ENST00000681901.1:c.*2326G>A	ENSP00000504883.1:n.*2326G>A
ENST00000368471.7:c.1841G>A	ENSP00000357456.3:p.Cys614Tyr
ENST00000368474.8:c.2726G>A	ENSP00000357459.4:p.Cys909Tyr
ENST00000529168.1:c.2633G>A	ENSP00000431794.1:p.Cys878Tyr
NM_001025107.2:c.1841G>A	NP_001020278.1:p.Cys614Tyr
NM_001111.4:c.2726G>A	NP_001102.2:p.Cys909Tyr
NM_001193495.1:c.1841G>A	NP_001180424.1:p.Cys614Tyr
NM_015840.3:c.2648G>A	NP_056655.2:p.Cys883Tyr
NM_015841.3:c.2591G>A	NP_056656.2:p.Cys864Tyr
XM_006711109.1:c.2756G>A	XP_006711172.1:p.Cys919Tyr
XM_006711111.2:c.1841G>A	XP_006711174.1:p.Cys614Tyr
XM_006711112.1:c.1841G>A	XP_006711175.1:p.Cys614Tyr
XM_006711113.1:c.1841G>A	XP_006711176.1:p.Cys614Tyr
XM_011509060.1:c.2855G>A	XP_011507362.1:p.Cys952Tyr
XM_011509061.1:c.2777G>A	XP_011507363.1:p.Cys926Tyr
XM_011509062.1:c.2744G>A	XP_011507364.1:p.Cys915Tyr
NM_001025107.3:c.1841G>A	NP_001020278.1:p.Cys614Tyr
NM_001111.5:c.2726G>A MANE Select	NP_001102.3:p.Cys909Tyr
NM_001193495.2:c.1841G>A	NP_001180424.1:p.Cys614Tyr
NM_001365045.1:c.2753G>A	NP_001351974.1:p.Cys918Tyr
NM_001365046.1:c.1841G>A	NP_001351975.1:p.Cys614Tyr
NM_001365047.1:c.1841G>A	NP_001351976.1:p.Cys614Tyr
NM_001365048.1:c.1841G>A	NP_001351977.1:p.Cys614Tyr
NM_001365049.1:c.1763G>A	NP_001351978.1:p.Cys588Tyr
NM_015840.4:c.2648G>A	NP_056655.3:p.Cys883Tyr
NM_015841.4:c.2591G>A	NP_056656.3:p.Cys864Tyr
XM_006711113.2:c.1841G>A	XP_006711176.1:p.Cys614Tyr
XM_011509061.2:c.1763G>A	XP_011507363.2:p.Cys588Tyr
XM_024449674.1:c.2855G>A	XP_024305442.1:p.Cys952Tyr