Canonical Allele Identifier: CA2480933209

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589793A= , CM000663.2:g.154589793A=	GRCh38
NC_000001.10:g.154562269A= , CM000663.1:g.154562269A=	GRCh37
NC_000001.9:g.152828893A=	NCBI36
NG_011844.1:g.43169T=
NG_011844.2:g.46768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2526T=	ENSP00000497790.2:n.2526T=
ENST00000649724.2:c.2662T=	ENSP00000497932.2:p.Ser888=
ENST00000680270.2:c.2515T=	ENSP00000505532.2:p.Ser839=
ENST00000681056.2:c.2284T=	ENSP00000506234.2:p.Ser762=
ENST00000368471.8:c.1747T=	ENSP00000357456.3:p.Ser583=
ENST00000368474.9:c.2632T= MANE Select	ENSP00000357459.4:p.Ser878=
ENST00000529168.2:c.2554T=	ENSP00000431794.2:p.Ser852=
ENST00000647682.2:n.2617T=
ENST00000648231.2:c.1747T=	ENSP00000497555.1:p.Ser583=
ENST00000648311.1:c.1747T=	ENSP00000498137.1:p.Ser583=
ENST00000648714.2:c.*107T=	ENSP00000497434.2:n.*107T=
ENST00000649021.1:n.2668T=
ENST00000649022.2:c.1747T=	ENSP00000496896.2:p.Ser583=
ENST00000649042.1:c.1747T=	ENSP00000497790.1:p.Ser583=
ENST00000649408.2:c.2632T=	ENSP00000497386.2:p.Ser878=
ENST00000649724.1:c.1747T=	ENSP00000497932.1:p.Ser583=
ENST00000649749.1:c.1747T=	ENSP00000497210.1:p.Ser583=
ENST00000679375.1:c.*864T=	ENSP00000505887.1:n.*864T=
ENST00000679465.1:n.3085T=
ENST00000679805.1:n.2668T=
ENST00000679899.1:c.1690T=	ENSP00000505996.1:p.Ser564=
ENST00000680270.1:c.1747T=	ENSP00000505532.1:p.Ser583=
ENST00000680305.1:c.2632T=	ENSP00000506312.1:p.Ser878=
ENST00000681056.1:c.1747T=	ENSP00000506234.1:p.Ser583=
ENST00000681235.1:c.*2154T=	ENSP00000506606.1:n.*2154T=
ENST00000681429.1:n.1892T=
ENST00000681683.1:c.1747T=	ENSP00000506666.1:p.Ser583=
ENST00000681786.1:n.3085T=
ENST00000681901.1:c.*2232T=	ENSP00000504883.1:n.*2232T=
ENST00000368471.7:c.1747T=	ENSP00000357456.3:p.Ser583=
ENST00000368474.8:c.2632T=	ENSP00000357459.4:p.Ser878=
ENST00000529168.1:c.2539T=	ENSP00000431794.1:p.Ser847=
NM_001025107.2:c.1747T=	NP_001020278.1:p.Ser583=
NM_001111.4:c.2632T=	NP_001102.2:p.Ser878=
NM_001193495.1:c.1747T=	NP_001180424.1:p.Ser583=
NM_015840.3:c.2554T=	NP_056655.2:p.Ser852=
NM_015841.3:c.2497T=	NP_056656.2:p.Ser833=
XM_006711109.1:c.2662T=	XP_006711172.1:p.Ser888=
XM_006711111.2:c.1747T=	XP_006711174.1:p.Ser583=
XM_006711112.1:c.1747T=	XP_006711175.1:p.Ser583=
XM_006711113.1:c.1747T=	XP_006711176.1:p.Ser583=
XM_011509060.1:c.2761T=	XP_011507362.1:p.Ser921=
XM_011509061.1:c.2683T=	XP_011507363.1:p.Ser895=
XM_011509062.1:c.2650T=	XP_011507364.1:p.Ser884=
NM_001025107.3:c.1747T=	NP_001020278.1:p.Ser583=
NM_001111.5:c.2632T= MANE Select	NP_001102.3:p.Ser878=
NM_001193495.2:c.1747T=	NP_001180424.1:p.Ser583=
NM_001365045.1:c.2659T=	NP_001351974.1:p.Ser887=
NM_001365046.1:c.1747T=	NP_001351975.1:p.Ser583=
NM_001365047.1:c.1747T=	NP_001351976.1:p.Ser583=
NM_001365048.1:c.1747T=	NP_001351977.1:p.Ser583=
NM_001365049.1:c.1669T=	NP_001351978.1:p.Ser557=
NM_015840.4:c.2554T=	NP_056655.3:p.Ser852=
NM_015841.4:c.2497T=	NP_056656.3:p.Ser833=
XM_006711113.2:c.1747T=	XP_006711176.1:p.Ser583=
XM_011509061.2:c.1669T=	XP_011507363.2:p.Ser557=
XM_024449674.1:c.2761T=	XP_024305442.1:p.Ser921=