Canonical Allele Identifier: CA421231414

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154557360T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154584884T>C , CM000663.2:g.154584884T>C	GRCh38
NC_000001.10:g.154557360T>C , CM000663.1:g.154557360T>C	GRCh37
NC_000001.9:g.152823984T>C	NCBI36
NG_011844.1:g.48078A>G
NG_011844.2:g.51677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.3497A>G	ENSP00000497790.2:n.3497A>G
ENST00000649724.2:c.3633A>G	ENSP00000497932.2:p.Lys1211=
ENST00000680270.2:c.3486A>G	ENSP00000505532.2:p.Lys1162=
ENST00000681056.2:c.3255A>G	ENSP00000506234.2:p.Lys1085=
ENST00000368471.8:c.2718A>G	ENSP00000357456.3:p.Lys906=
ENST00000368474.9:c.3603A>G MANE Select	ENSP00000357459.4:p.Lys1201=
ENST00000492630.2:n.2396A>G
ENST00000529168.2:c.3525A>G	ENSP00000431794.2:p.Lys1175=
ENST00000647682.2:n.3588A>G
ENST00000648231.2:c.2718A>G	ENSP00000497555.1:p.Lys906=
ENST00000648311.1:c.2718A>G	ENSP00000498137.1:p.Lys906=
ENST00000648714.2:c.*1078A>G	ENSP00000497434.2:n.*1078A>G
ENST00000649021.1:n.4339A>G
ENST00000649022.2:c.2718A>G	ENSP00000496896.2:p.Lys906=
ENST00000649042.1:c.2718A>G	ENSP00000497790.1:p.Lys906=
ENST00000649408.2:c.*769A>G	ENSP00000497386.2:n.*769A>G
ENST00000649724.1:c.2718A>G	ENSP00000497932.1:p.Lys906=
ENST00000649749.1:c.2718A>G	ENSP00000497210.1:p.Lys906=
ENST00000679375.1:c.*1835A>G	ENSP00000505887.1:n.*1835A>G
ENST00000679465.1:n.4464A>G
ENST00000679805.1:n.4339A>G
ENST00000679899.1:c.2661A>G	ENSP00000505996.1:p.Lys887=
ENST00000680270.1:c.2718A>G	ENSP00000505532.1:p.Lys906=
ENST00000680305.1:c.3420A>G	ENSP00000506312.1:p.Lys1140=
ENST00000681056.1:c.2718A>G	ENSP00000506234.1:p.Lys906=
ENST00000681235.1:c.*3125A>G	ENSP00000506606.1:n.*3125A>G
ENST00000681429.1:n.3271A>G
ENST00000681683.1:c.2718A>G	ENSP00000506666.1:p.Lys906=
ENST00000681786.1:n.4464A>G
ENST00000681901.1:c.*3203A>G	ENSP00000504883.1:n.*3203A>G
ENST00000368471.7:c.2718A>G	ENSP00000357456.3:p.Lys906=
ENST00000368474.8:c.3603A>G	ENSP00000357459.4:p.Lys1201=
ENST00000492630.1:n.362A>G
ENST00000529168.1:c.3510A>G	ENSP00000431794.1:p.Lys1170=
NM_001025107.2:c.2718A>G	NP_001020278.1:p.Lys906=
NM_001111.4:c.3603A>G	NP_001102.2:p.Lys1201=
NM_001193495.1:c.2718A>G	NP_001180424.1:p.Lys906=
NM_015840.3:c.3525A>G	NP_056655.2:p.Lys1175=
NM_015841.3:c.3468A>G	NP_056656.2:p.Lys1156=
XM_006711109.1:c.3633A>G	XP_006711172.1:p.Lys1211=
XM_006711111.2:c.2718A>G	XP_006711174.1:p.Lys906=
XM_006711112.1:c.2718A>G	XP_006711175.1:p.Lys906=
XM_006711113.1:c.2718A>G	XP_006711176.1:p.Lys906=
XM_011509060.1:c.3732A>G	XP_011507362.1:p.Lys1244=
XM_011509061.1:c.3654A>G	XP_011507363.1:p.Lys1218=
XM_011509062.1:c.3621A>G	XP_011507364.1:p.Lys1207=
NM_001025107.3:c.2718A>G	NP_001020278.1:p.Lys906=
NM_001111.5:c.3603A>G MANE Select	NP_001102.3:p.Lys1201=
NM_001193495.2:c.2718A>G	NP_001180424.1:p.Lys906=
NM_001365045.1:c.3630A>G	NP_001351974.1:p.Lys1210=
NM_001365046.1:c.2718A>G	NP_001351975.1:p.Lys906=
NM_001365047.1:c.2718A>G	NP_001351976.1:p.Lys906=
NM_001365048.1:c.2718A>G	NP_001351977.1:p.Lys906=
NM_001365049.1:c.2640A>G	NP_001351978.1:p.Lys880=
NM_015840.4:c.3525A>G	NP_056655.3:p.Lys1175=
NM_015841.4:c.3468A>G	NP_056656.3:p.Lys1156=
XM_006711113.2:c.2718A>G	XP_006711176.1:p.Lys906=
XM_011509061.2:c.2640A>G	XP_011507363.2:p.Lys880=
XM_024449674.1:c.3732A>G	XP_024305442.1:p.Lys1244=