Canonical Allele Identifier: CA413722488

Gene: ATRX

Linked Data

• dbSNP Id: rs1057518708
• MyVariant Identifiers: chrX:g.76944336G>T (hg19) ; chrX:g.77688843G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77688843G>T , CM000685.2:g.77688843G>T	GRCh38
NC_000023.10:g.76944336G>T , CM000685.1:g.76944336G>T	GRCh37
NC_000023.9:g.76830992G>T	NCBI36
NG_008838.2:g.102379C>A
NG_008838.3:g.102427C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.569C>A MANE Select	ENSP00000362441.4:p.Pro190His
ENST00000373344.9:c.569C>A	ENSP00000362441.4:p.Pro190His
ENST00000395603.7:c.455C>A	ENSP00000378967.3:p.Pro152His
ENST00000480283.5:c.*197C>A	ENSP00000480196.1:n.*197C>A
ENST00000623321.3:c.404C>A	ENSP00000485127.1:p.Pro135His
ENST00000624032.3:c.569C>A	ENSP00000485253.1:p.Pro190His
ENST00000624166.3:c.452C>A	ENSP00000485103.1:p.Pro151His
ENST00000624668.3:c.290C>A	ENSP00000485100.1:p.Pro97His
ENST00000625063.3:c.384C>A
NM_000489.4:c.569C>A	NP_000480.3:p.Pro190His
NM_138270.3:c.455C>A	NP_612114.2:p.Pro152His
XM_005262153.3:c.566C>A	XP_005262210.2:p.Pro189His
XM_005262154.3:c.569C>A	XP_005262211.2:p.Pro190His
XM_005262155.3:c.452C>A	XP_005262212.2:p.Pro151His
XM_005262156.3:c.404C>A	XP_005262213.2:p.Pro135His
XM_005262157.3:c.452C>A	XP_005262214.2:p.Pro151His
XM_006724666.2:c.452C>A	XP_006724729.1:p.Pro151His
XM_006724667.2:c.290C>A	XP_006724730.1:p.Pro97His
XM_006724668.2:c.569C>A	XP_006724731.1:p.Pro190His
XR_938400.1:n.837C>A
NM_000489.5:c.569C>A	NP_000480.3:p.Pro190His
XM_005262153.5:c.566C>A	XP_005262210.2:p.Pro189His
XM_005262154.5:c.569C>A	XP_005262211.2:p.Pro190His
XM_005262155.4:c.452C>A	XP_005262212.2:p.Pro151His
XM_005262156.4:c.404C>A	XP_005262213.2:p.Pro135His
XM_005262157.5:c.452C>A	XP_005262214.2:p.Pro151His
XM_006724666.4:c.452C>A	XP_006724729.1:p.Pro151His
XM_006724667.3:c.290C>A	XP_006724730.1:p.Pro97His
XM_006724668.3:c.569C>A	XP_006724731.1:p.Pro190His
XM_017029601.2:c.566C>A	XP_016885090.1:p.Pro189His
XM_017029602.1:c.449C>A	XP_016885091.1:p.Pro150His
XM_017029603.1:c.401C>A	XP_016885092.1:p.Pro134His
XM_017029604.2:c.455C>A	XP_016885093.1:p.Pro152His
XM_017029605.1:c.452C>A	XP_016885094.1:p.Pro151His
XM_017029606.2:c.338C>A	XP_016885095.1:p.Pro113His
XM_017029607.2:c.335C>A	XP_016885096.1:p.Pro112His
XM_017029608.2:c.287C>A	XP_016885097.1:p.Pro96His
XM_017029609.1:c.338C>A	XP_016885098.1:p.Pro113His
XM_017029610.1:c.335C>A	XP_016885099.1:p.Pro112His
XM_017029611.1:c.290C>A	XP_016885100.1:p.Pro97His
XR_001755700.2:n.794C>A
NM_138270.4:c.455C>A	NP_612114.2:p.Pro152His
NM_000489.6:c.569C>A MANE Select	NP_000480.3:p.Pro190His
NM_138270.5:c.455C>A	NP_612114.2:p.Pro152His