Canonical Allele Identifier: CA413708311

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907726T>C (hg19) ; chrX:g.77652236T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652236T>C , CM000685.2:g.77652236T>C	GRCh38
NC_000023.10:g.76907726T>C , CM000685.1:g.76907726T>C	GRCh37
NC_000023.9:g.76794382T>C	NCBI36
NG_008838.2:g.138986A>G
NG_008838.3:g.139034A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4435A>G MANE Select	ENSP00000362441.4:p.Lys1479Glu
ENST00000373344.9:c.4435A>G	ENSP00000362441.4:p.Lys1479Glu
ENST00000395603.7:c.4321A>G	ENSP00000378967.3:p.Lys1441Glu
ENST00000480283.5:c.*4063A>G	ENSP00000480196.1:n.*4063A>G
ENST00000623242.3:c.41A>G
NM_000489.4:c.4435A>G	NP_000480.3:p.Lys1479Glu
NM_138270.3:c.4321A>G	NP_612114.2:p.Lys1441Glu
XM_005262153.3:c.4432A>G	XP_005262210.2:p.Lys1478Glu
XM_005262154.3:c.4348A>G	XP_005262211.2:p.Lys1450Glu
XM_005262155.3:c.4318A>G	XP_005262212.2:p.Lys1440Glu
XM_005262156.3:c.4270A>G	XP_005262213.2:p.Lys1424Glu
XM_005262157.3:c.4231A>G	XP_005262214.2:p.Lys1411Glu
XM_006724666.2:c.4318A>G	XP_006724729.1:p.Lys1440Glu
XM_006724667.2:c.4156A>G	XP_006724730.1:p.Lys1386Glu
XM_006724668.2:c.4435A>G	XP_006724731.1:p.Lys1479Glu
XR_938400.1:n.4703A>G
NM_000489.5:c.4435A>G	NP_000480.3:p.Lys1479Glu
XM_005262153.5:c.4432A>G	XP_005262210.2:p.Lys1478Glu
XM_005262154.5:c.4348A>G	XP_005262211.2:p.Lys1450Glu
XM_005262155.4:c.4318A>G	XP_005262212.2:p.Lys1440Glu
XM_005262156.4:c.4270A>G	XP_005262213.2:p.Lys1424Glu
XM_005262157.5:c.4231A>G	XP_005262214.2:p.Lys1411Glu
XM_006724666.4:c.4318A>G	XP_006724729.1:p.Lys1440Glu
XM_006724667.3:c.4156A>G	XP_006724730.1:p.Lys1386Glu
XM_006724668.3:c.4435A>G	XP_006724731.1:p.Lys1479Glu
XM_017029601.2:c.4345A>G	XP_016885090.1:p.Lys1449Glu
XM_017029602.1:c.4315A>G	XP_016885091.1:p.Lys1439Glu
XM_017029603.1:c.4267A>G	XP_016885092.1:p.Lys1423Glu
XM_017029604.2:c.4234A>G	XP_016885093.1:p.Lys1412Glu
XM_017029605.1:c.4231A>G	XP_016885094.1:p.Lys1411Glu
XM_017029606.2:c.4204A>G	XP_016885095.1:p.Lys1402Glu
XM_017029607.2:c.4201A>G	XP_016885096.1:p.Lys1401Glu
XM_017029608.2:c.4153A>G	XP_016885097.1:p.Lys1385Glu
XM_017029609.1:c.4117A>G	XP_016885098.1:p.Lys1373Glu
XM_017029610.1:c.4114A>G	XP_016885099.1:p.Lys1372Glu
XM_017029611.1:c.4069A>G	XP_016885100.1:p.Lys1357Glu
XR_001755700.2:n.4660A>G
NM_138270.4:c.4321A>G	NP_612114.2:p.Lys1441Glu
NM_000489.6:c.4435A>G MANE Select	NP_000480.3:p.Lys1479Glu
NM_138270.5:c.4321A>G	NP_612114.2:p.Lys1441Glu