Canonical Allele Identifier: CA413708820

Gene: ATRX

Linked Data

• dbSNP Id: rs2148439905
• MyVariant Identifiers: chrX:g.76907804C>G (hg19) ; chrX:g.77652314C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652314C>G , CM000685.2:g.77652314C>G	GRCh38
NC_000023.10:g.76907804C>G , CM000685.1:g.76907804C>G	GRCh37
NC_000023.9:g.76794460C>G	NCBI36
NG_008838.2:g.138908G>C
NG_008838.3:g.138956G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4357G>C MANE Select	ENSP00000362441.4:p.Glu1453Gln
ENST00000373344.9:c.4357G>C	ENSP00000362441.4:p.Glu1453Gln
ENST00000395603.7:c.4243G>C	ENSP00000378967.3:p.Glu1415Gln
ENST00000480283.5:c.*3985G>C	ENSP00000480196.1:n.*3985G>C
NM_000489.4:c.4357G>C	NP_000480.3:p.Glu1453Gln
NM_138270.3:c.4243G>C	NP_612114.2:p.Glu1415Gln
XM_005262153.3:c.4354G>C	XP_005262210.2:p.Glu1452Gln
XM_005262154.3:c.4270G>C	XP_005262211.2:p.Glu1424Gln
XM_005262155.3:c.4240G>C	XP_005262212.2:p.Glu1414Gln
XM_005262156.3:c.4192G>C	XP_005262213.2:p.Glu1398Gln
XM_005262157.3:c.4153G>C	XP_005262214.2:p.Glu1385Gln
XM_006724666.2:c.4240G>C	XP_006724729.1:p.Glu1414Gln
XM_006724667.2:c.4078G>C	XP_006724730.1:p.Glu1360Gln
XM_006724668.2:c.4357G>C	XP_006724731.1:p.Glu1453Gln
XR_938400.1:n.4625G>C
NM_000489.5:c.4357G>C	NP_000480.3:p.Glu1453Gln
XM_005262153.5:c.4354G>C	XP_005262210.2:p.Glu1452Gln
XM_005262154.5:c.4270G>C	XP_005262211.2:p.Glu1424Gln
XM_005262155.4:c.4240G>C	XP_005262212.2:p.Glu1414Gln
XM_005262156.4:c.4192G>C	XP_005262213.2:p.Glu1398Gln
XM_005262157.5:c.4153G>C	XP_005262214.2:p.Glu1385Gln
XM_006724666.4:c.4240G>C	XP_006724729.1:p.Glu1414Gln
XM_006724667.3:c.4078G>C	XP_006724730.1:p.Glu1360Gln
XM_006724668.3:c.4357G>C	XP_006724731.1:p.Glu1453Gln
XM_017029601.2:c.4267G>C	XP_016885090.1:p.Glu1423Gln
XM_017029602.1:c.4237G>C	XP_016885091.1:p.Glu1413Gln
XM_017029603.1:c.4189G>C	XP_016885092.1:p.Glu1397Gln
XM_017029604.2:c.4156G>C	XP_016885093.1:p.Glu1386Gln
XM_017029605.1:c.4153G>C	XP_016885094.1:p.Glu1385Gln
XM_017029606.2:c.4126G>C	XP_016885095.1:p.Glu1376Gln
XM_017029607.2:c.4123G>C	XP_016885096.1:p.Glu1375Gln
XM_017029608.2:c.4075G>C	XP_016885097.1:p.Glu1359Gln
XM_017029609.1:c.4039G>C	XP_016885098.1:p.Glu1347Gln
XM_017029610.1:c.4036G>C	XP_016885099.1:p.Glu1346Gln
XM_017029611.1:c.3991G>C	XP_016885100.1:p.Glu1331Gln
XR_001755700.2:n.4582G>C
NM_138270.4:c.4243G>C	NP_612114.2:p.Glu1415Gln
NM_000489.6:c.4357G>C MANE Select	NP_000480.3:p.Glu1453Gln
NM_138270.5:c.4243G>C	NP_612114.2:p.Glu1415Gln