Canonical Allele Identifier: CA421231964

Gene: ADAR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588216G>A , CM000663.2:g.154588216G>A	GRCh38
NC_000001.10:g.154560692G>A , CM000663.1:g.154560692G>A	GRCh37
NC_000001.9:g.152827316G>A	NCBI36
NG_011844.1:g.44746C>T
NG_011844.2:g.48345C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2822C>T	ENSP00000497790.2:n.2822C>T
ENST00000649724.2:c.2958C>T	ENSP00000497932.2:p.Cys986=
ENST00000680270.2:c.2811C>T	ENSP00000505532.2:p.Cys937=
ENST00000681056.2:c.2580C>T	ENSP00000506234.2:p.Cys860=
ENST00000368471.8:c.2043C>T	ENSP00000357456.3:p.Cys681=
ENST00000368474.9:c.2928C>T MANE Select	ENSP00000357459.4:p.Cys976=
ENST00000529168.2:c.2850C>T	ENSP00000431794.2:p.Cys950=
ENST00000647682.2:n.2913C>T
ENST00000648231.2:c.2043C>T	ENSP00000497555.1:p.Cys681=
ENST00000648311.1:c.2043C>T	ENSP00000498137.1:p.Cys681=
ENST00000648714.2:c.*403C>T	ENSP00000497434.2:n.*403C>T
ENST00000649021.1:n.3256C>T
ENST00000649022.2:c.2043C>T	ENSP00000496896.2:p.Cys681=
ENST00000649042.1:c.2043C>T	ENSP00000497790.1:p.Cys681=
ENST00000649408.2:c.2928C>T	ENSP00000497386.2:p.Cys976=
ENST00000649724.1:c.2043C>T	ENSP00000497932.1:p.Cys681=
ENST00000649749.1:c.2043C>T	ENSP00000497210.1:p.Cys681=
ENST00000679375.1:c.*1160C>T	ENSP00000505887.1:n.*1160C>T
ENST00000679465.1:n.3381C>T
ENST00000679805.1:n.3256C>T
ENST00000679899.1:c.1986C>T	ENSP00000505996.1:p.Cys662=
ENST00000680270.1:c.2043C>T	ENSP00000505532.1:p.Cys681=
ENST00000680305.1:c.2928C>T	ENSP00000506312.1:p.Cys976=
ENST00000681056.1:c.2043C>T	ENSP00000506234.1:p.Cys681=
ENST00000681235.1:c.*2450C>T	ENSP00000506606.1:n.*2450C>T
ENST00000681429.1:n.2188C>T
ENST00000681683.1:c.2043C>T	ENSP00000506666.1:p.Cys681=
ENST00000681786.1:n.3381C>T
ENST00000681901.1:c.*2528C>T	ENSP00000504883.1:n.*2528C>T
ENST00000368471.7:c.2043C>T	ENSP00000357456.3:p.Cys681=
ENST00000368474.8:c.2928C>T	ENSP00000357459.4:p.Cys976=
ENST00000529168.1:c.2835C>T	ENSP00000431794.1:p.Cys945=
ENST00000530954.1:n.65C>T
ENST00000534279.1:n.387C>T
NM_001025107.2:c.2043C>T	NP_001020278.1:p.Cys681=
NM_001111.4:c.2928C>T	NP_001102.2:p.Cys976=
NM_001193495.1:c.2043C>T	NP_001180424.1:p.Cys681=
NM_015840.3:c.2850C>T	NP_056655.2:p.Cys950=
NM_015841.3:c.2793C>T	NP_056656.2:p.Cys931=
XM_006711109.1:c.2958C>T	XP_006711172.1:p.Cys986=
XM_006711111.2:c.2043C>T	XP_006711174.1:p.Cys681=
XM_006711112.1:c.2043C>T	XP_006711175.1:p.Cys681=
XM_006711113.1:c.2043C>T	XP_006711176.1:p.Cys681=
XM_011509060.1:c.3057C>T	XP_011507362.1:p.Cys1019=
XM_011509061.1:c.2979C>T	XP_011507363.1:p.Cys993=
XM_011509062.1:c.2946C>T	XP_011507364.1:p.Cys982=
NM_001025107.3:c.2043C>T	NP_001020278.1:p.Cys681=
NM_001111.5:c.2928C>T MANE Select	NP_001102.3:p.Cys976=
NM_001193495.2:c.2043C>T	NP_001180424.1:p.Cys681=
NM_001365045.1:c.2955C>T	NP_001351974.1:p.Cys985=
NM_001365046.1:c.2043C>T	NP_001351975.1:p.Cys681=
NM_001365047.1:c.2043C>T	NP_001351976.1:p.Cys681=
NM_001365048.1:c.2043C>T	NP_001351977.1:p.Cys681=
NM_001365049.1:c.1965C>T	NP_001351978.1:p.Cys655=
NM_015840.4:c.2850C>T	NP_056655.3:p.Cys950=
NM_015841.4:c.2793C>T	NP_056656.3:p.Cys931=
XM_006711113.2:c.2043C>T	XP_006711176.1:p.Cys681=
XM_011509061.2:c.1965C>T	XP_011507363.2:p.Cys655=
XM_024449674.1:c.3057C>T	XP_024305442.1:p.Cys1019=