Canonical Allele Identifier: CA420975172

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154561862G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589386G>A , CM000663.2:g.154589386G>A	GRCh38
NC_000001.10:g.154561862G>A , CM000663.1:g.154561862G>A	GRCh37
NC_000001.9:g.152828486G>A	NCBI36
NG_011844.1:g.43576C>T
NG_011844.2:g.47175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2639C>T	ENSP00000497790.2:n.2639C>T
ENST00000649724.2:c.2775C>T	ENSP00000497932.2:p.Ser925=
ENST00000680270.2:c.2628C>T	ENSP00000505532.2:p.Ser876=
ENST00000681056.2:c.2397C>T	ENSP00000506234.2:p.Ser799=
ENST00000368471.8:c.1860C>T	ENSP00000357456.3:p.Ser620=
ENST00000368474.9:c.2745C>T MANE Select	ENSP00000357459.4:p.Ser915=
ENST00000529168.2:c.2667C>T	ENSP00000431794.2:p.Ser889=
ENST00000647682.2:n.2730C>T
ENST00000648231.2:c.1860C>T	ENSP00000497555.1:p.Ser620=
ENST00000648311.1:c.1860C>T	ENSP00000498137.1:p.Ser620=
ENST00000648714.2:c.*220C>T	ENSP00000497434.2:n.*220C>T
ENST00000649021.1:n.2781C>T
ENST00000649022.2:c.1860C>T	ENSP00000496896.2:p.Ser620=
ENST00000649042.1:c.1860C>T	ENSP00000497790.1:p.Ser620=
ENST00000649408.2:c.2745C>T	ENSP00000497386.2:p.Ser915=
ENST00000649724.1:c.1860C>T	ENSP00000497932.1:p.Ser620=
ENST00000649749.1:c.1860C>T	ENSP00000497210.1:p.Ser620=
ENST00000679375.1:c.*977C>T	ENSP00000505887.1:n.*977C>T
ENST00000679465.1:n.3198C>T
ENST00000679805.1:n.2781C>T
ENST00000679899.1:c.1803C>T	ENSP00000505996.1:p.Ser601=
ENST00000680270.1:c.1860C>T	ENSP00000505532.1:p.Ser620=
ENST00000680305.1:c.2745C>T	ENSP00000506312.1:p.Ser915=
ENST00000681056.1:c.1860C>T	ENSP00000506234.1:p.Ser620=
ENST00000681235.1:c.*2267C>T	ENSP00000506606.1:n.*2267C>T
ENST00000681429.1:n.2005C>T
ENST00000681683.1:c.1860C>T	ENSP00000506666.1:p.Ser620=
ENST00000681786.1:n.3198C>T
ENST00000681901.1:c.*2345C>T	ENSP00000504883.1:n.*2345C>T
ENST00000368471.7:c.1860C>T	ENSP00000357456.3:p.Ser620=
ENST00000368474.8:c.2745C>T	ENSP00000357459.4:p.Ser915=
ENST00000529168.1:c.2652C>T	ENSP00000431794.1:p.Ser884=
NM_001025107.2:c.1860C>T	NP_001020278.1:p.Ser620=
NM_001111.4:c.2745C>T	NP_001102.2:p.Ser915=
NM_001193495.1:c.1860C>T	NP_001180424.1:p.Ser620=
NM_015840.3:c.2667C>T	NP_056655.2:p.Ser889=
NM_015841.3:c.2610C>T	NP_056656.2:p.Ser870=
XM_006711109.1:c.2775C>T	XP_006711172.1:p.Ser925=
XM_006711111.2:c.1860C>T	XP_006711174.1:p.Ser620=
XM_006711112.1:c.1860C>T	XP_006711175.1:p.Ser620=
XM_006711113.1:c.1860C>T	XP_006711176.1:p.Ser620=
XM_011509060.1:c.2874C>T	XP_011507362.1:p.Ser958=
XM_011509061.1:c.2796C>T	XP_011507363.1:p.Ser932=
XM_011509062.1:c.2763C>T	XP_011507364.1:p.Ser921=
NM_001025107.3:c.1860C>T	NP_001020278.1:p.Ser620=
NM_001111.5:c.2745C>T MANE Select	NP_001102.3:p.Ser915=
NM_001193495.2:c.1860C>T	NP_001180424.1:p.Ser620=
NM_001365045.1:c.2772C>T	NP_001351974.1:p.Ser924=
NM_001365046.1:c.1860C>T	NP_001351975.1:p.Ser620=
NM_001365047.1:c.1860C>T	NP_001351976.1:p.Ser620=
NM_001365048.1:c.1860C>T	NP_001351977.1:p.Ser620=
NM_001365049.1:c.1782C>T	NP_001351978.1:p.Ser594=
NM_015840.4:c.2667C>T	NP_056655.3:p.Ser889=
NM_015841.4:c.2610C>T	NP_056656.3:p.Ser870=
XM_006711113.2:c.1860C>T	XP_006711176.1:p.Ser620=
XM_011509061.2:c.1782C>T	XP_011507363.2:p.Ser594=
XM_024449674.1:c.2874C>T	XP_024305442.1:p.Ser958=