Canonical Allele Identifier: CA342636845

Gene: ADAR

Linked Data

• MyVariant Identifiers: chr1:g.154562280A>G (hg19) ; chr1:g.154589804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154589804A>G , CM000663.2:g.154589804A>G	GRCh38
NC_000001.10:g.154562280A>G , CM000663.1:g.154562280A>G	GRCh37
NC_000001.9:g.152828904A>G	NCBI36
NG_011844.1:g.43158T>C
NG_011844.2:g.46757T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649042.2:c.2515T>C	ENSP00000497790.2:n.2515T>C
ENST00000649724.2:c.2651T>C	ENSP00000497932.2:p.Met884Thr
ENST00000680270.2:c.2504T>C	ENSP00000505532.2:p.Met835Thr
ENST00000681056.2:c.2273T>C	ENSP00000506234.2:p.Met758Thr
ENST00000368471.8:c.1736T>C	ENSP00000357456.3:p.Met579Thr
ENST00000368474.9:c.2621T>C MANE Select	ENSP00000357459.4:p.Met874Thr
ENST00000529168.2:c.2543T>C	ENSP00000431794.2:p.Met848Thr
ENST00000647682.2:n.2606T>C
ENST00000648231.2:c.1736T>C	ENSP00000497555.1:p.Met579Thr
ENST00000648311.1:c.1736T>C	ENSP00000498137.1:p.Met579Thr
ENST00000648714.2:c.*96T>C	ENSP00000497434.2:n.*96T>C
ENST00000649021.1:n.2657T>C
ENST00000649022.2:c.1736T>C	ENSP00000496896.2:p.Met579Thr
ENST00000649042.1:c.1736T>C	ENSP00000497790.1:p.Met579Thr
ENST00000649408.2:c.2621T>C	ENSP00000497386.2:p.Met874Thr
ENST00000649724.1:c.1736T>C	ENSP00000497932.1:p.Met579Thr
ENST00000649749.1:c.1736T>C	ENSP00000497210.1:p.Met579Thr
ENST00000679375.1:c.*853T>C	ENSP00000505887.1:n.*853T>C
ENST00000679465.1:n.3074T>C
ENST00000679805.1:n.2657T>C
ENST00000679899.1:c.1679T>C	ENSP00000505996.1:p.Met560Thr
ENST00000680270.1:c.1736T>C	ENSP00000505532.1:p.Met579Thr
ENST00000680305.1:c.2621T>C	ENSP00000506312.1:p.Met874Thr
ENST00000681056.1:c.1736T>C	ENSP00000506234.1:p.Met579Thr
ENST00000681235.1:c.*2143T>C	ENSP00000506606.1:n.*2143T>C
ENST00000681429.1:n.1881T>C
ENST00000681683.1:c.1736T>C	ENSP00000506666.1:p.Met579Thr
ENST00000681786.1:n.3074T>C
ENST00000681901.1:c.*2221T>C	ENSP00000504883.1:n.*2221T>C
ENST00000368471.7:c.1736T>C	ENSP00000357456.3:p.Met579Thr
ENST00000368474.8:c.2621T>C	ENSP00000357459.4:p.Met874Thr
ENST00000529168.1:c.2528T>C	ENSP00000431794.1:p.Met843Thr
NM_001025107.2:c.1736T>C	NP_001020278.1:p.Met579Thr
NM_001111.4:c.2621T>C	NP_001102.2:p.Met874Thr
NM_001193495.1:c.1736T>C	NP_001180424.1:p.Met579Thr
NM_015840.3:c.2543T>C	NP_056655.2:p.Met848Thr
NM_015841.3:c.2486T>C	NP_056656.2:p.Met829Thr
XM_006711109.1:c.2651T>C	XP_006711172.1:p.Met884Thr
XM_006711111.2:c.1736T>C	XP_006711174.1:p.Met579Thr
XM_006711112.1:c.1736T>C	XP_006711175.1:p.Met579Thr
XM_006711113.1:c.1736T>C	XP_006711176.1:p.Met579Thr
XM_011509060.1:c.2750T>C	XP_011507362.1:p.Met917Thr
XM_011509061.1:c.2672T>C	XP_011507363.1:p.Met891Thr
XM_011509062.1:c.2639T>C	XP_011507364.1:p.Met880Thr
NM_001025107.3:c.1736T>C	NP_001020278.1:p.Met579Thr
NM_001111.5:c.2621T>C MANE Select	NP_001102.3:p.Met874Thr
NM_001193495.2:c.1736T>C	NP_001180424.1:p.Met579Thr
NM_001365045.1:c.2648T>C	NP_001351974.1:p.Met883Thr
NM_001365046.1:c.1736T>C	NP_001351975.1:p.Met579Thr
NM_001365047.1:c.1736T>C	NP_001351976.1:p.Met579Thr
NM_001365048.1:c.1736T>C	NP_001351977.1:p.Met579Thr
NM_001365049.1:c.1658T>C	NP_001351978.1:p.Met553Thr
NM_015840.4:c.2543T>C	NP_056655.3:p.Met848Thr
NM_015841.4:c.2486T>C	NP_056656.3:p.Met829Thr
XM_006711113.2:c.1736T>C	XP_006711176.1:p.Met579Thr
XM_011509061.2:c.1658T>C	XP_011507363.2:p.Met553Thr
XM_024449674.1:c.2750T>C	XP_024305442.1:p.Met917Thr