Canonical Allele Identifier: CA342636114

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154560690C>A (hg19) ; chr1:g.154588214C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154588214C>A , CM000663.2:g.154588214C>A	GRCh38
NC_000001.10:g.154560690C>A , CM000663.1:g.154560690C>A	GRCh37
NC_000001.9:g.152827314C>A	NCBI36
NG_011844.1:g.44748G>T
NG_011844.2:g.48347G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2824G>T	ENSP00000497790.2:n.2824G>T
ENST00000649724.2:c.2960G>T	ENSP00000497932.2:p.Ser987Ile
ENST00000680270.2:c.2813G>T	ENSP00000505532.2:p.Ser938Ile
ENST00000681056.2:c.2582G>T	ENSP00000506234.2:p.Ser861Ile
ENST00000368471.8:c.2045G>T	ENSP00000357456.3:p.Ser682Ile
ENST00000368474.9:c.2930G>T MANE Select	ENSP00000357459.4:p.Ser977Ile
ENST00000529168.2:c.2852G>T	ENSP00000431794.2:p.Ser951Ile
ENST00000647682.2:n.2915G>T
ENST00000648231.2:c.2045G>T	ENSP00000497555.1:p.Ser682Ile
ENST00000648311.1:c.2045G>T	ENSP00000498137.1:p.Ser682Ile
ENST00000648714.2:c.*405G>T	ENSP00000497434.2:n.*405G>T
ENST00000649021.1:n.3258G>T
ENST00000649022.2:c.2045G>T	ENSP00000496896.2:p.Ser682Ile
ENST00000649042.1:c.2045G>T	ENSP00000497790.1:p.Ser682Ile
ENST00000649408.2:c.2930G>T	ENSP00000497386.2:p.Ser977Ile
ENST00000649724.1:c.2045G>T	ENSP00000497932.1:p.Ser682Ile
ENST00000649749.1:c.2045G>T	ENSP00000497210.1:p.Ser682Ile
ENST00000679375.1:c.*1162G>T	ENSP00000505887.1:n.*1162G>T
ENST00000679465.1:n.3383G>T
ENST00000679805.1:n.3258G>T
ENST00000679899.1:c.1988G>T	ENSP00000505996.1:p.Ser663Ile
ENST00000680270.1:c.2045G>T	ENSP00000505532.1:p.Ser682Ile
ENST00000680305.1:c.2930G>T	ENSP00000506312.1:p.Ser977Ile
ENST00000681056.1:c.2045G>T	ENSP00000506234.1:p.Ser682Ile
ENST00000681235.1:c.*2452G>T	ENSP00000506606.1:n.*2452G>T
ENST00000681429.1:n.2190G>T
ENST00000681683.1:c.2045G>T	ENSP00000506666.1:p.Ser682Ile
ENST00000681786.1:n.3383G>T
ENST00000681901.1:c.*2530G>T	ENSP00000504883.1:n.*2530G>T
ENST00000368471.7:c.2045G>T	ENSP00000357456.3:p.Ser682Ile
ENST00000368474.8:c.2930G>T	ENSP00000357459.4:p.Ser977Ile
ENST00000529168.1:c.2837G>T	ENSP00000431794.1:p.Ser946Ile
ENST00000530954.1:n.67G>T
ENST00000534279.1:n.389G>T
NM_001025107.2:c.2045G>T	NP_001020278.1:p.Ser682Ile
NM_001111.4:c.2930G>T	NP_001102.2:p.Ser977Ile
NM_001193495.1:c.2045G>T	NP_001180424.1:p.Ser682Ile
NM_015840.3:c.2852G>T	NP_056655.2:p.Ser951Ile
NM_015841.3:c.2795G>T	NP_056656.2:p.Ser932Ile
XM_006711109.1:c.2960G>T	XP_006711172.1:p.Ser987Ile
XM_006711111.2:c.2045G>T	XP_006711174.1:p.Ser682Ile
XM_006711112.1:c.2045G>T	XP_006711175.1:p.Ser682Ile
XM_006711113.1:c.2045G>T	XP_006711176.1:p.Ser682Ile
XM_011509060.1:c.3059G>T	XP_011507362.1:p.Ser1020Ile
XM_011509061.1:c.2981G>T	XP_011507363.1:p.Ser994Ile
XM_011509062.1:c.2948G>T	XP_011507364.1:p.Ser983Ile
NM_001025107.3:c.2045G>T	NP_001020278.1:p.Ser682Ile
NM_001111.5:c.2930G>T MANE Select	NP_001102.3:p.Ser977Ile
NM_001193495.2:c.2045G>T	NP_001180424.1:p.Ser682Ile
NM_001365045.1:c.2957G>T	NP_001351974.1:p.Ser986Ile
NM_001365046.1:c.2045G>T	NP_001351975.1:p.Ser682Ile
NM_001365047.1:c.2045G>T	NP_001351976.1:p.Ser682Ile
NM_001365048.1:c.2045G>T	NP_001351977.1:p.Ser682Ile
NM_001365049.1:c.1967G>T	NP_001351978.1:p.Ser656Ile
NM_015840.4:c.2852G>T	NP_056655.3:p.Ser951Ile
NM_015841.4:c.2795G>T	NP_056656.3:p.Ser932Ile
XM_006711113.2:c.2045G>T	XP_006711176.1:p.Ser682Ile
XM_011509061.2:c.1967G>T	XP_011507363.2:p.Ser656Ile
XM_024449674.1:c.3059G>T	XP_024305442.1:p.Ser1020Ile