Canonical Allele Identifier: CA526406504

Gene: ADAR

Linked Data

• dbSNP Id: rs894073890
• gnomAD v2: 1-154587697-ATTTT-A
• gnomAD v3: 1-154615221-ATTTT-A
• gnomAD v4: 1-154615221-ATTTT-A
• MyVariant Identifiers: chr1:g.154587698_154587701del (hg19) ; chr1:g.154615222_154615225del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154615225_154615228del , CM000663.2:g.154615225_154615228del	GRCh38
NC_000001.10:g.154587701_154587704del , CM000663.1:g.154587701_154587704del	GRCh37
NC_000001.9:g.152854325_152854328del	NCBI36
NG_011844.1:g.17737_17740del
NG_011844.2:g.21336_21339del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.46-12599_46-12596del	ENSP00000497790.2:n.46-12599_46-12596del
ENST00000649724.2:c.46-12599_46-12596del	ENSP00000497932.2:n.46-12599_46-12596del
ENST00000680270.2:c.46-12599_46-12596del	ENSP00000505532.2:n.46-12599_46-12596del
ENST00000681056.2:c.45+12729_45+12732del	ENSP00000506234.2:n.45+12729_45+12732del
ENST00000368471.8:c.-870-12599_-870-12596del	ENSP00000357456.3:n.-870-12599_-870-12596del
ENST00000471068.2:n.148+12211_148+12214del
ENST00000648311.1:c.-871+12211_-871+12214del	ENSP00000498137.1:n.-871+12211_-871+12214del
ENST00000649021.1:n.52-12599_52-12596del
ENST00000649022.2:c.-871+9838_-871+9841del	ENSP00000496896.2:n.-871+9838_-871+9841del
ENST00000649042.1:c.-734-12599_-734-12596del	ENSP00000497790.1:n.-734-12599_-734-12596del
ENST00000649724.1:c.-870-12599_-870-12596del	ENSP00000497932.1:n.-870-12599_-870-12596del
ENST00000679375.1:c.-493+12630_-493+12633del	ENSP00000505887.1:n.-493+12630_-493+12633del
ENST00000679805.1:n.52-12599_52-12596del
ENST00000679899.1:c.-870-12599_-870-12596del	ENSP00000505996.1:n.-870-12599_-870-12596del
ENST00000680270.1:c.-723-12599_-723-12596del	ENSP00000505532.1:n.-723-12599_-723-12596del
ENST00000680472.1:n.55-12599_55-12596del
ENST00000681056.1:c.-493+12729_-493+12732del	ENSP00000506234.1:n.-493+12729_-493+12732del
ENST00000681683.1:c.-734-12599_-734-12596del	ENSP00000506666.1:n.-734-12599_-734-12596del
ENST00000368471.7:c.-870-12599_-870-12596del	ENSP00000357456.3:n.-870-12599_-870-12596del
ENST00000463920.5:n.34-12599_34-12596del
ENST00000471068.1:n.47-12599_47-12596del
ENST00000494866.1:n.59-12599_59-12596del
NM_001025107.2:c.-870-12599_-870-12596del	NP_001020278.1:n.-870-12599_-870-12596del
XM_006711109.1:c.46-12599_46-12596del	XP_006711172.1:n.46-12599_46-12596del
XM_006711112.1:c.-734-12599_-734-12596del	XP_006711175.1:n.-734-12599_-734-12596del
XM_006711113.1:c.-734-12599_-734-12596del	XP_006711176.1:n.-734-12599_-734-12596del
XM_011509060.1:c.145-12599_145-12596del	XP_011507362.1:n.145-12599_145-12596del
XM_011509061.1:c.145-12599_145-12596del	XP_011507363.1:n.145-12599_145-12596del
XM_011509062.1:c.33+9838_33+9841del	XP_011507364.1:n.33+9838_33+9841del
NM_001025107.3:c.-870-12599_-870-12596del	NP_001020278.1:n.-870-12599_-870-12596del
NM_001365045.1:c.43-12599_43-12596del	NP_001351974.1:n.43-12599_43-12596del
NM_001365046.1:c.-734-12599_-734-12596del	NP_001351975.1:n.-734-12599_-734-12596del
XM_006711113.2:c.-734-12599_-734-12596del	XP_006711176.1:n.-734-12599_-734-12596del
XM_011509061.2:c.-870-12599_-870-12596del	XP_011507363.2:n.-870-12599_-870-12596del
XM_024449674.1:c.145-12599_145-12596del	XP_024305442.1:n.145-12599_145-12596del