Canonical Allele Identifier: CA413701282

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829817C>A (hg19) ; chrX:g.77574352C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574352C>A , CM000685.2:g.77574352C>A	GRCh38
NC_000023.10:g.76829817C>A , CM000685.1:g.76829817C>A	GRCh37
NC_000023.9:g.76716473C>A	NCBI36
NG_008838.2:g.216870G>T
NG_008838.3:g.216918G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6224G>T MANE Select	ENSP00000362441.4:p.Gly2075Val
ENST00000636152.1:n.59G>T
ENST00000675732.1:c.1322G>T	ENSP00000502598.1:p.Gly441Val
ENST00000373344.9:c.6224G>T	ENSP00000362441.4:p.Gly2075Val
ENST00000395603.7:c.6110G>T	ENSP00000378967.3:p.Gly2037Val
ENST00000480283.5:c.*5852G>T	ENSP00000480196.1:n.*5852G>T
ENST00000623316.1:c.708G>T
ENST00000623706.3:n.3294G>T
NM_000489.4:c.6224G>T	NP_000480.3:p.Gly2075Val
NM_138270.3:c.6110G>T	NP_612114.2:p.Gly2037Val
XM_005262153.3:c.6221G>T	XP_005262210.2:p.Gly2074Val
XM_005262154.3:c.6137G>T	XP_005262211.2:p.Gly2046Val
XM_005262155.3:c.6107G>T	XP_005262212.2:p.Gly2036Val
XM_005262156.3:c.6059G>T	XP_005262213.2:p.Gly2020Val
XM_005262157.3:c.6020G>T	XP_005262214.2:p.Gly2007Val
XM_006724666.2:c.6107G>T	XP_006724729.1:p.Gly2036Val
XM_006724667.2:c.5945G>T	XP_006724730.1:p.Gly1982Val
XR_938400.1:n.6566G>T
NM_000489.5:c.6224G>T	NP_000480.3:p.Gly2075Val
XM_005262153.5:c.6221G>T	XP_005262210.2:p.Gly2074Val
XM_005262154.5:c.6137G>T	XP_005262211.2:p.Gly2046Val
XM_005262155.4:c.6107G>T	XP_005262212.2:p.Gly2036Val
XM_005262156.4:c.6059G>T	XP_005262213.2:p.Gly2020Val
XM_005262157.5:c.6020G>T	XP_005262214.2:p.Gly2007Val
XM_006724666.4:c.6107G>T	XP_006724729.1:p.Gly2036Val
XM_006724667.3:c.5945G>T	XP_006724730.1:p.Gly1982Val
XM_017029601.2:c.6134G>T	XP_016885090.1:p.Gly2045Val
XM_017029602.1:c.6104G>T	XP_016885091.1:p.Gly2035Val
XM_017029603.1:c.6056G>T	XP_016885092.1:p.Gly2019Val
XM_017029604.2:c.6023G>T	XP_016885093.1:p.Gly2008Val
XM_017029605.1:c.6020G>T	XP_016885094.1:p.Gly2007Val
XM_017029606.2:c.5993G>T	XP_016885095.1:p.Gly1998Val
XM_017029607.2:c.5990G>T	XP_016885096.1:p.Gly1997Val
XM_017029608.2:c.5942G>T	XP_016885097.1:p.Gly1981Val
XM_017029609.1:c.5906G>T	XP_016885098.1:p.Gly1969Val
XM_017029610.1:c.5903G>T	XP_016885099.1:p.Gly1968Val
XM_017029611.1:c.5858G>T	XP_016885100.1:p.Gly1953Val
XR_001755700.2:n.6523G>T
NM_138270.4:c.6110G>T	NP_612114.2:p.Gly2037Val
NM_000489.6:c.6224G>T MANE Select	NP_000480.3:p.Gly2075Val
NM_138270.5:c.6110G>T	NP_612114.2:p.Gly2037Val