Canonical Allele Identifier: CA413708702

Gene: ATRX

Linked Data

• dbSNP Id: rs2148439350
• MyVariant Identifiers: chrX:g.76907786C>G (hg19) ; chrX:g.77652296C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652296C>G , CM000685.2:g.77652296C>G	GRCh38
NC_000023.10:g.76907786C>G , CM000685.1:g.76907786C>G	GRCh37
NC_000023.9:g.76794442C>G	NCBI36
NG_008838.2:g.138926G>C
NG_008838.3:g.138974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4375G>C MANE Select	ENSP00000362441.4:p.Glu1459Gln
ENST00000373344.9:c.4375G>C	ENSP00000362441.4:p.Glu1459Gln
ENST00000395603.7:c.4261G>C	ENSP00000378967.3:p.Glu1421Gln
ENST00000480283.5:c.*4003G>C	ENSP00000480196.1:n.*4003G>C
NM_000489.4:c.4375G>C	NP_000480.3:p.Glu1459Gln
NM_138270.3:c.4261G>C	NP_612114.2:p.Glu1421Gln
XM_005262153.3:c.4372G>C	XP_005262210.2:p.Glu1458Gln
XM_005262154.3:c.4288G>C	XP_005262211.2:p.Glu1430Gln
XM_005262155.3:c.4258G>C	XP_005262212.2:p.Glu1420Gln
XM_005262156.3:c.4210G>C	XP_005262213.2:p.Glu1404Gln
XM_005262157.3:c.4171G>C	XP_005262214.2:p.Glu1391Gln
XM_006724666.2:c.4258G>C	XP_006724729.1:p.Glu1420Gln
XM_006724667.2:c.4096G>C	XP_006724730.1:p.Glu1366Gln
XM_006724668.2:c.4375G>C	XP_006724731.1:p.Glu1459Gln
XR_938400.1:n.4643G>C
NM_000489.5:c.4375G>C	NP_000480.3:p.Glu1459Gln
XM_005262153.5:c.4372G>C	XP_005262210.2:p.Glu1458Gln
XM_005262154.5:c.4288G>C	XP_005262211.2:p.Glu1430Gln
XM_005262155.4:c.4258G>C	XP_005262212.2:p.Glu1420Gln
XM_005262156.4:c.4210G>C	XP_005262213.2:p.Glu1404Gln
XM_005262157.5:c.4171G>C	XP_005262214.2:p.Glu1391Gln
XM_006724666.4:c.4258G>C	XP_006724729.1:p.Glu1420Gln
XM_006724667.3:c.4096G>C	XP_006724730.1:p.Glu1366Gln
XM_006724668.3:c.4375G>C	XP_006724731.1:p.Glu1459Gln
XM_017029601.2:c.4285G>C	XP_016885090.1:p.Glu1429Gln
XM_017029602.1:c.4255G>C	XP_016885091.1:p.Glu1419Gln
XM_017029603.1:c.4207G>C	XP_016885092.1:p.Glu1403Gln
XM_017029604.2:c.4174G>C	XP_016885093.1:p.Glu1392Gln
XM_017029605.1:c.4171G>C	XP_016885094.1:p.Glu1391Gln
XM_017029606.2:c.4144G>C	XP_016885095.1:p.Glu1382Gln
XM_017029607.2:c.4141G>C	XP_016885096.1:p.Glu1381Gln
XM_017029608.2:c.4093G>C	XP_016885097.1:p.Glu1365Gln
XM_017029609.1:c.4057G>C	XP_016885098.1:p.Glu1353Gln
XM_017029610.1:c.4054G>C	XP_016885099.1:p.Glu1352Gln
XM_017029611.1:c.4009G>C	XP_016885100.1:p.Glu1337Gln
XR_001755700.2:n.4600G>C
NM_138270.4:c.4261G>C	NP_612114.2:p.Glu1421Gln
NM_000489.6:c.4375G>C MANE Select	NP_000480.3:p.Glu1459Gln
NM_138270.5:c.4261G>C	NP_612114.2:p.Glu1421Gln