Canonical Allele Identifier: CA421231435

Gene: ADAR

Linked Data

• gnomAD v4: 1-154584899-C-T
• MyVariant Identifiers: chr1:g.154557375C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584899C>T , CM000663.2:g.154584899C>T	GRCh38
NC_000001.10:g.154557375C>T , CM000663.1:g.154557375C>T	GRCh37
NC_000001.9:g.152823999C>T	NCBI36
NG_011844.1:g.48063G>A
NG_011844.2:g.51662G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3482G>A	ENSP00000497790.2:n.3482G>A
ENST00000649724.2:c.3618G>A	ENSP00000497932.2:p.Lys1206=
ENST00000680270.2:c.3471G>A	ENSP00000505532.2:p.Lys1157=
ENST00000681056.2:c.3240G>A	ENSP00000506234.2:p.Lys1080=
ENST00000368471.8:c.2703G>A	ENSP00000357456.3:p.Lys901=
ENST00000368474.9:c.3588G>A MANE Select	ENSP00000357459.4:p.Lys1196=
ENST00000492630.2:n.2381G>A
ENST00000529168.2:c.3510G>A	ENSP00000431794.2:p.Lys1170=
ENST00000647682.2:n.3573G>A
ENST00000648231.2:c.2703G>A	ENSP00000497555.1:p.Lys901=
ENST00000648311.1:c.2703G>A	ENSP00000498137.1:p.Lys901=
ENST00000648714.2:c.*1063G>A	ENSP00000497434.2:n.*1063G>A
ENST00000649021.1:n.4324G>A
ENST00000649022.2:c.2703G>A	ENSP00000496896.2:p.Lys901=
ENST00000649042.1:c.2703G>A	ENSP00000497790.1:p.Lys901=
ENST00000649408.2:c.*754G>A	ENSP00000497386.2:n.*754G>A
ENST00000649724.1:c.2703G>A	ENSP00000497932.1:p.Lys901=
ENST00000649749.1:c.2703G>A	ENSP00000497210.1:p.Lys901=
ENST00000679375.1:c.*1820G>A	ENSP00000505887.1:n.*1820G>A
ENST00000679465.1:n.4449G>A
ENST00000679805.1:n.4324G>A
ENST00000679899.1:c.2646G>A	ENSP00000505996.1:p.Lys882=
ENST00000680270.1:c.2703G>A	ENSP00000505532.1:p.Lys901=
ENST00000680305.1:c.3405G>A	ENSP00000506312.1:p.Lys1135=
ENST00000681056.1:c.2703G>A	ENSP00000506234.1:p.Lys901=
ENST00000681235.1:c.*3110G>A	ENSP00000506606.1:n.*3110G>A
ENST00000681429.1:n.3256G>A
ENST00000681683.1:c.2703G>A	ENSP00000506666.1:p.Lys901=
ENST00000681786.1:n.4449G>A
ENST00000681901.1:c.*3188G>A	ENSP00000504883.1:n.*3188G>A
ENST00000368471.7:c.2703G>A	ENSP00000357456.3:p.Lys901=
ENST00000368474.8:c.3588G>A	ENSP00000357459.4:p.Lys1196=
ENST00000492630.1:n.347G>A
ENST00000529168.1:c.3495G>A	ENSP00000431794.1:p.Lys1165=
NM_001025107.2:c.2703G>A	NP_001020278.1:p.Lys901=
NM_001111.4:c.3588G>A	NP_001102.2:p.Lys1196=
NM_001193495.1:c.2703G>A	NP_001180424.1:p.Lys901=
NM_015840.3:c.3510G>A	NP_056655.2:p.Lys1170=
NM_015841.3:c.3453G>A	NP_056656.2:p.Lys1151=
XM_006711109.1:c.3618G>A	XP_006711172.1:p.Lys1206=
XM_006711111.2:c.2703G>A	XP_006711174.1:p.Lys901=
XM_006711112.1:c.2703G>A	XP_006711175.1:p.Lys901=
XM_006711113.1:c.2703G>A	XP_006711176.1:p.Lys901=
XM_011509060.1:c.3717G>A	XP_011507362.1:p.Lys1239=
XM_011509061.1:c.3639G>A	XP_011507363.1:p.Lys1213=
XM_011509062.1:c.3606G>A	XP_011507364.1:p.Lys1202=
NM_001025107.3:c.2703G>A	NP_001020278.1:p.Lys901=
NM_001111.5:c.3588G>A MANE Select	NP_001102.3:p.Lys1196=
NM_001193495.2:c.2703G>A	NP_001180424.1:p.Lys901=
NM_001365045.1:c.3615G>A	NP_001351974.1:p.Lys1205=
NM_001365046.1:c.2703G>A	NP_001351975.1:p.Lys901=
NM_001365047.1:c.2703G>A	NP_001351976.1:p.Lys901=
NM_001365048.1:c.2703G>A	NP_001351977.1:p.Lys901=
NM_001365049.1:c.2625G>A	NP_001351978.1:p.Lys875=
NM_015840.4:c.3510G>A	NP_056655.3:p.Lys1170=
NM_015841.4:c.3453G>A	NP_056656.3:p.Lys1151=
XM_006711113.2:c.2703G>A	XP_006711176.1:p.Lys901=
XM_011509061.2:c.2625G>A	XP_011507363.2:p.Lys875=
XM_024449674.1:c.3717G>A	XP_024305442.1:p.Lys1239=