Canonical Allele Identifier: CA421231441

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557381C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584905C>G , CM000663.2:g.154584905C>G	GRCh38
NC_000001.10:g.154557381C>G , CM000663.1:g.154557381C>G	GRCh37
NC_000001.9:g.152824005C>G	NCBI36
NG_011844.1:g.48057G>C
NG_011844.2:g.51656G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000649042.2:c.3476G>C	ENSP00000497790.2:n.3476G>C
ENST00000649724.2:c.3612G>C	ENSP00000497932.2:p.Thr1204=
ENST00000680270.2:c.3465G>C	ENSP00000505532.2:p.Thr1155=
ENST00000681056.2:c.3234G>C	ENSP00000506234.2:p.Thr1078=
ENST00000368471.8:c.2697G>C	ENSP00000357456.3:p.Thr899=
ENST00000368474.9:c.3582G>C MANE Select	ENSP00000357459.4:p.Thr1194=
ENST00000492630.2:n.2375G>C
ENST00000529168.2:c.3504G>C	ENSP00000431794.2:p.Thr1168=
ENST00000647682.2:n.3567G>C
ENST00000648231.2:c.2697G>C	ENSP00000497555.1:p.Thr899=
ENST00000648311.1:c.2697G>C	ENSP00000498137.1:p.Thr899=
ENST00000648714.2:c.*1057G>C	ENSP00000497434.2:n.*1057G>C
ENST00000649021.1:n.4318G>C
ENST00000649022.2:c.2697G>C	ENSP00000496896.2:p.Thr899=
ENST00000649042.1:c.2697G>C	ENSP00000497790.1:p.Thr899=
ENST00000649408.2:c.*748G>C	ENSP00000497386.2:n.*748G>C
ENST00000649724.1:c.2697G>C	ENSP00000497932.1:p.Thr899=
ENST00000649749.1:c.2697G>C	ENSP00000497210.1:p.Thr899=
ENST00000679375.1:c.*1814G>C	ENSP00000505887.1:n.*1814G>C
ENST00000679465.1:n.4443G>C
ENST00000679805.1:n.4318G>C
ENST00000679899.1:c.2640G>C	ENSP00000505996.1:p.Thr880=
ENST00000680270.1:c.2697G>C	ENSP00000505532.1:p.Thr899=
ENST00000680305.1:c.3399G>C	ENSP00000506312.1:p.Thr1133=
ENST00000681056.1:c.2697G>C	ENSP00000506234.1:p.Thr899=
ENST00000681235.1:c.*3104G>C	ENSP00000506606.1:n.*3104G>C
ENST00000681429.1:n.3250G>C
ENST00000681683.1:c.2697G>C	ENSP00000506666.1:p.Thr899=
ENST00000681786.1:n.4443G>C
ENST00000681901.1:c.*3182G>C	ENSP00000504883.1:n.*3182G>C
ENST00000368471.7:c.2697G>C	ENSP00000357456.3:p.Thr899=
ENST00000368474.8:c.3582G>C	ENSP00000357459.4:p.Thr1194=
ENST00000492630.1:n.341G>C
ENST00000529168.1:c.3489G>C	ENSP00000431794.1:p.Thr1163=
NM_001025107.2:c.2697G>C	NP_001020278.1:p.Thr899=
NM_001111.4:c.3582G>C	NP_001102.2:p.Thr1194=
NM_001193495.1:c.2697G>C	NP_001180424.1:p.Thr899=
NM_015840.3:c.3504G>C	NP_056655.2:p.Thr1168=
NM_015841.3:c.3447G>C	NP_056656.2:p.Thr1149=
XM_006711109.1:c.3612G>C	XP_006711172.1:p.Thr1204=
XM_006711111.2:c.2697G>C	XP_006711174.1:p.Thr899=
XM_006711112.1:c.2697G>C	XP_006711175.1:p.Thr899=
XM_006711113.1:c.2697G>C	XP_006711176.1:p.Thr899=
XM_011509060.1:c.3711G>C	XP_011507362.1:p.Thr1237=
XM_011509061.1:c.3633G>C	XP_011507363.1:p.Thr1211=
XM_011509062.1:c.3600G>C	XP_011507364.1:p.Thr1200=
NM_001025107.3:c.2697G>C	NP_001020278.1:p.Thr899=
NM_001111.5:c.3582G>C MANE Select	NP_001102.3:p.Thr1194=
NM_001193495.2:c.2697G>C	NP_001180424.1:p.Thr899=
NM_001365045.1:c.3609G>C	NP_001351974.1:p.Thr1203=
NM_001365046.1:c.2697G>C	NP_001351975.1:p.Thr899=
NM_001365047.1:c.2697G>C	NP_001351976.1:p.Thr899=
NM_001365048.1:c.2697G>C	NP_001351977.1:p.Thr899=
NM_001365049.1:c.2619G>C	NP_001351978.1:p.Thr873=
NM_015840.4:c.3504G>C	NP_056655.3:p.Thr1168=
NM_015841.4:c.3447G>C	NP_056656.3:p.Thr1149=
XM_006711113.2:c.2697G>C	XP_006711176.1:p.Thr899=
XM_011509061.2:c.2619G>C	XP_011507363.2:p.Thr873=
XM_024449674.1:c.3711G>C	XP_024305442.1:p.Thr1237=