Canonical Allele Identifier: CA2480944408

Gene: ADAR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154615205_154615206delinsCA , CM000663.2:g.154615205_154615206delinsCA	GRCh38
NC_000001.10:g.154587681_154587682delinsCA , CM000663.1:g.154587681_154587682delinsCA	GRCh37
NC_000001.9:g.152854305_152854306delinsCA	NCBI36
NG_011844.1:g.17756_17757delinsTG
NG_011844.2:g.21355_21356delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.46-12580_46-12579delinsTG	ENSP00000497790.2:n.46-12580_46-12579delinsTG
ENST00000649724.2:c.46-12580_46-12579delinsTG	ENSP00000497932.2:n.46-12580_46-12579delinsTG
ENST00000680270.2:c.46-12580_46-12579delinsTG	ENSP00000505532.2:n.46-12580_46-12579delinsTG
ENST00000681056.2:c.45+12748_45+12749delinsTG	ENSP00000506234.2:n.45+12748_45+12749delinsTG
ENST00000368471.8:c.-870-12580_-870-12579delinsTG	ENSP00000357456.3:n.-870-12580_-870-12579delinsTG
ENST00000471068.2:n.148+12230_148+12231delinsTG
ENST00000648311.1:c.-871+12230_-871+12231delinsTG	ENSP00000498137.1:n.-871+12230_-871+12231delinsTG
ENST00000649021.1:n.52-12580_52-12579delinsTG
ENST00000649022.2:c.-871+9857_-871+9858delinsTG	ENSP00000496896.2:n.-871+9857_-871+9858delinsTG
ENST00000649042.1:c.-734-12580_-734-12579delinsTG	ENSP00000497790.1:n.-734-12580_-734-12579delinsTG
ENST00000649724.1:c.-870-12580_-870-12579delinsTG	ENSP00000497932.1:n.-870-12580_-870-12579delinsTG
ENST00000679375.1:c.-493+12649_-493+12650delinsTG	ENSP00000505887.1:n.-493+12649_-493+12650delinsTG
ENST00000679805.1:n.52-12580_52-12579delinsTG
ENST00000679899.1:c.-870-12580_-870-12579delinsTG	ENSP00000505996.1:n.-870-12580_-870-12579delinsTG
ENST00000680270.1:c.-723-12580_-723-12579delinsTG	ENSP00000505532.1:n.-723-12580_-723-12579delinsTG
ENST00000680472.1:n.55-12580_55-12579delinsTG
ENST00000681056.1:c.-493+12748_-493+12749delinsTG	ENSP00000506234.1:n.-493+12748_-493+12749delinsTG
ENST00000681683.1:c.-734-12580_-734-12579delinsTG	ENSP00000506666.1:n.-734-12580_-734-12579delinsTG
ENST00000368471.7:c.-870-12580_-870-12579delinsTG	ENSP00000357456.3:n.-870-12580_-870-12579delinsTG
ENST00000463920.5:n.34-12580_34-12579delinsTG
ENST00000471068.1:n.47-12580_47-12579delinsTG
ENST00000494866.1:n.59-12580_59-12579delinsTG
NM_001025107.2:c.-870-12580_-870-12579delinsTG	NP_001020278.1:n.-870-12580_-870-12579delinsTG
XM_006711109.1:c.46-12580_46-12579delinsTG	XP_006711172.1:n.46-12580_46-12579delinsTG
XM_006711112.1:c.-734-12580_-734-12579delinsTG	XP_006711175.1:n.-734-12580_-734-12579delinsTG
XM_006711113.1:c.-734-12580_-734-12579delinsTG	XP_006711176.1:n.-734-12580_-734-12579delinsTG
XM_011509060.1:c.145-12580_145-12579delinsTG	XP_011507362.1:n.145-12580_145-12579delinsTG
XM_011509061.1:c.145-12580_145-12579delinsTG	XP_011507363.1:n.145-12580_145-12579delinsTG
XM_011509062.1:c.33+9857_33+9858delinsTG	XP_011507364.1:n.33+9857_33+9858delinsTG
NM_001025107.3:c.-870-12580_-870-12579delinsTG	NP_001020278.1:n.-870-12580_-870-12579delinsTG
NM_001365045.1:c.43-12580_43-12579delinsTG	NP_001351974.1:n.43-12580_43-12579delinsTG
NM_001365046.1:c.-734-12580_-734-12579delinsTG	NP_001351975.1:n.-734-12580_-734-12579delinsTG
XM_006711113.2:c.-734-12580_-734-12579delinsTG	XP_006711176.1:n.-734-12580_-734-12579delinsTG
XM_011509061.2:c.-870-12580_-870-12579delinsTG	XP_011507363.2:n.-870-12580_-870-12579delinsTG
XM_024449674.1:c.145-12580_145-12579delinsTG	XP_024305442.1:n.145-12580_145-12579delinsTG