Canonical Allele Identifier: CA413704826

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76889194T>C (hg19) ; chrX:g.77633706T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77633706T>C , CM000685.2:g.77633706T>C	GRCh38
NC_000023.10:g.76889194T>C , CM000685.1:g.76889194T>C	GRCh37
NC_000023.9:g.76775850T>C	NCBI36
NG_008838.2:g.157516A>G
NG_008838.3:g.157564A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4816A>G MANE Select	ENSP00000362441.4:p.Ser1606Gly
ENST00000675732.1:c.-87A>G	ENSP00000502598.1:n.-87A>G
ENST00000675908.1:n.551A>G
ENST00000373344.9:c.4816A>G	ENSP00000362441.4:p.Ser1606Gly
ENST00000395603.7:c.4702A>G	ENSP00000378967.3:p.Ser1568Gly
ENST00000480283.5:c.*4444A>G	ENSP00000480196.1:n.*4444A>G
ENST00000623242.3:c.553A>G
ENST00000624403.1:n.160A>G
NM_000489.4:c.4816A>G	NP_000480.3:p.Ser1606Gly
NM_138270.3:c.4702A>G	NP_612114.2:p.Ser1568Gly
XM_005262153.3:c.4813A>G	XP_005262210.2:p.Ser1605Gly
XM_005262154.3:c.4729A>G	XP_005262211.2:p.Ser1577Gly
XM_005262155.3:c.4699A>G	XP_005262212.2:p.Ser1567Gly
XM_005262156.3:c.4651A>G	XP_005262213.2:p.Ser1551Gly
XM_005262157.3:c.4612A>G	XP_005262214.2:p.Ser1538Gly
XM_006724666.2:c.4699A>G	XP_006724729.1:p.Ser1567Gly
XM_006724667.2:c.4537A>G	XP_006724730.1:p.Ser1513Gly
XM_006724668.2:c.4816A>G	XP_006724731.1:p.Ser1606Gly
XR_938400.1:n.5084A>G
NM_000489.5:c.4816A>G	NP_000480.3:p.Ser1606Gly
XM_005262153.5:c.4813A>G	XP_005262210.2:p.Ser1605Gly
XM_005262154.5:c.4729A>G	XP_005262211.2:p.Ser1577Gly
XM_005262155.4:c.4699A>G	XP_005262212.2:p.Ser1567Gly
XM_005262156.4:c.4651A>G	XP_005262213.2:p.Ser1551Gly
XM_005262157.5:c.4612A>G	XP_005262214.2:p.Ser1538Gly
XM_006724666.4:c.4699A>G	XP_006724729.1:p.Ser1567Gly
XM_006724667.3:c.4537A>G	XP_006724730.1:p.Ser1513Gly
XM_006724668.3:c.4816A>G	XP_006724731.1:p.Ser1606Gly
XM_017029601.2:c.4726A>G	XP_016885090.1:p.Ser1576Gly
XM_017029602.1:c.4696A>G	XP_016885091.1:p.Ser1566Gly
XM_017029603.1:c.4648A>G	XP_016885092.1:p.Ser1550Gly
XM_017029604.2:c.4615A>G	XP_016885093.1:p.Ser1539Gly
XM_017029605.1:c.4612A>G	XP_016885094.1:p.Ser1538Gly
XM_017029606.2:c.4585A>G	XP_016885095.1:p.Ser1529Gly
XM_017029607.2:c.4582A>G	XP_016885096.1:p.Ser1528Gly
XM_017029608.2:c.4534A>G	XP_016885097.1:p.Ser1512Gly
XM_017029609.1:c.4498A>G	XP_016885098.1:p.Ser1500Gly
XM_017029610.1:c.4495A>G	XP_016885099.1:p.Ser1499Gly
XM_017029611.1:c.4450A>G	XP_016885100.1:p.Ser1484Gly
XR_001755700.2:n.5041A>G
NM_138270.4:c.4702A>G	NP_612114.2:p.Ser1568Gly
NM_000489.6:c.4816A>G MANE Select	NP_000480.3:p.Ser1606Gly
NM_138270.5:c.4702A>G	NP_612114.2:p.Ser1568Gly