Canonical Allele Identifier: CA421231640

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562288G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589812G>T , CM000663.2:g.154589812G>T	GRCh38
NC_000001.10:g.154562288G>T , CM000663.1:g.154562288G>T	GRCh37
NC_000001.9:g.152828912G>T	NCBI36
NG_011844.1:g.43150C>A
NG_011844.2:g.46749C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2507C>A	ENSP00000497790.2:n.2507C>A
ENST00000649724.2:c.2643C>A	ENSP00000497932.2:p.Ala881=
ENST00000680270.2:c.2496C>A	ENSP00000505532.2:p.Ala832=
ENST00000681056.2:c.2265C>A	ENSP00000506234.2:p.Ala755=
ENST00000368471.8:c.1728C>A	ENSP00000357456.3:p.Ala576=
ENST00000368474.9:c.2613C>A MANE Select	ENSP00000357459.4:p.Ala871=
ENST00000529168.2:c.2535C>A	ENSP00000431794.2:p.Ala845=
ENST00000647682.2:n.2598C>A
ENST00000648231.2:c.1728C>A	ENSP00000497555.1:p.Ala576=
ENST00000648311.1:c.1728C>A	ENSP00000498137.1:p.Ala576=
ENST00000648714.2:c.*88C>A	ENSP00000497434.2:n.*88C>A
ENST00000649021.1:n.2649C>A
ENST00000649022.2:c.1728C>A	ENSP00000496896.2:p.Ala576=
ENST00000649042.1:c.1728C>A	ENSP00000497790.1:p.Ala576=
ENST00000649408.2:c.2613C>A	ENSP00000497386.2:p.Ala871=
ENST00000649724.1:c.1728C>A	ENSP00000497932.1:p.Ala576=
ENST00000649749.1:c.1728C>A	ENSP00000497210.1:p.Ala576=
ENST00000679375.1:c.*845C>A	ENSP00000505887.1:n.*845C>A
ENST00000679465.1:n.3066C>A
ENST00000679805.1:n.2649C>A
ENST00000679899.1:c.1671C>A	ENSP00000505996.1:p.Ala557=
ENST00000680270.1:c.1728C>A	ENSP00000505532.1:p.Ala576=
ENST00000680305.1:c.2613C>A	ENSP00000506312.1:p.Ala871=
ENST00000681056.1:c.1728C>A	ENSP00000506234.1:p.Ala576=
ENST00000681235.1:c.*2135C>A	ENSP00000506606.1:n.*2135C>A
ENST00000681429.1:n.1873C>A
ENST00000681683.1:c.1728C>A	ENSP00000506666.1:p.Ala576=
ENST00000681786.1:n.3066C>A
ENST00000681901.1:c.*2213C>A	ENSP00000504883.1:n.*2213C>A
ENST00000368471.7:c.1728C>A	ENSP00000357456.3:p.Ala576=
ENST00000368474.8:c.2613C>A	ENSP00000357459.4:p.Ala871=
ENST00000529168.1:c.2520C>A	ENSP00000431794.1:p.Ala840=
NM_001025107.2:c.1728C>A	NP_001020278.1:p.Ala576=
NM_001111.4:c.2613C>A	NP_001102.2:p.Ala871=
NM_001193495.1:c.1728C>A	NP_001180424.1:p.Ala576=
NM_015840.3:c.2535C>A	NP_056655.2:p.Ala845=
NM_015841.3:c.2478C>A	NP_056656.2:p.Ala826=
XM_006711109.1:c.2643C>A	XP_006711172.1:p.Ala881=
XM_006711111.2:c.1728C>A	XP_006711174.1:p.Ala576=
XM_006711112.1:c.1728C>A	XP_006711175.1:p.Ala576=
XM_006711113.1:c.1728C>A	XP_006711176.1:p.Ala576=
XM_011509060.1:c.2742C>A	XP_011507362.1:p.Ala914=
XM_011509061.1:c.2664C>A	XP_011507363.1:p.Ala888=
XM_011509062.1:c.2631C>A	XP_011507364.1:p.Ala877=
NM_001025107.3:c.1728C>A	NP_001020278.1:p.Ala576=
NM_001111.5:c.2613C>A MANE Select	NP_001102.3:p.Ala871=
NM_001193495.2:c.1728C>A	NP_001180424.1:p.Ala576=
NM_001365045.1:c.2640C>A	NP_001351974.1:p.Ala880=
NM_001365046.1:c.1728C>A	NP_001351975.1:p.Ala576=
NM_001365047.1:c.1728C>A	NP_001351976.1:p.Ala576=
NM_001365048.1:c.1728C>A	NP_001351977.1:p.Ala576=
NM_001365049.1:c.1650C>A	NP_001351978.1:p.Ala550=
NM_015840.4:c.2535C>A	NP_056655.3:p.Ala845=
NM_015841.4:c.2478C>A	NP_056656.3:p.Ala826=
XM_006711113.2:c.1728C>A	XP_006711176.1:p.Ala576=
XM_011509061.2:c.1650C>A	XP_011507363.2:p.Ala550=
XM_024449674.1:c.2742C>A	XP_024305442.1:p.Ala914=