Canonical Allele Identifier: CA413703825

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763899G>T (hg19) ; chrX:g.77508421G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508421G>T , CM000685.2:g.77508421G>T	GRCh38
NC_000023.10:g.76763899G>T , CM000685.1:g.76763899G>T	GRCh37
NC_000023.9:g.76650555G>T	NCBI36
NG_008838.2:g.282801C>A
NG_008838.3:g.282849C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7409C>A MANE Select	ENSP00000362441.4:p.Pro2470Gln
ENST00000675732.1:c.2507C>A	ENSP00000502598.1:p.Pro836Gln
ENST00000373344.9:c.7409C>A	ENSP00000362441.4:p.Pro2470Gln
ENST00000395603.7:c.7295C>A	ENSP00000378967.3:p.Pro2432Gln
ENST00000480283.5:c.*7037C>A	ENSP00000480196.1:n.*7037C>A
ENST00000623706.3:n.5729C>A
NM_000489.4:c.7409C>A	NP_000480.3:p.Pro2470Gln
NM_138270.3:c.7295C>A	NP_612114.2:p.Pro2432Gln
XM_005262153.3:c.7406C>A	XP_005262210.2:p.Pro2469Gln
XM_005262154.3:c.7322C>A	XP_005262211.2:p.Pro2441Gln
XM_005262155.3:c.7292C>A	XP_005262212.2:p.Pro2431Gln
XM_005262156.3:c.7244C>A	XP_005262213.2:p.Pro2415Gln
XM_005262157.3:c.7205C>A	XP_005262214.2:p.Pro2402Gln
XM_006724666.2:c.7292C>A	XP_006724729.1:p.Pro2431Gln
XM_006724667.2:c.7130C>A	XP_006724730.1:p.Pro2377Gln
XR_938400.1:n.9001C>A
NM_000489.5:c.7409C>A	NP_000480.3:p.Pro2470Gln
XM_005262153.5:c.7406C>A	XP_005262210.2:p.Pro2469Gln
XM_005262154.5:c.7322C>A	XP_005262211.2:p.Pro2441Gln
XM_005262155.4:c.7292C>A	XP_005262212.2:p.Pro2431Gln
XM_005262156.4:c.7244C>A	XP_005262213.2:p.Pro2415Gln
XM_005262157.5:c.7205C>A	XP_005262214.2:p.Pro2402Gln
XM_006724666.4:c.7292C>A	XP_006724729.1:p.Pro2431Gln
XM_006724667.3:c.7130C>A	XP_006724730.1:p.Pro2377Gln
XM_017029601.2:c.7319C>A	XP_016885090.1:p.Pro2440Gln
XM_017029602.1:c.7289C>A	XP_016885091.1:p.Pro2430Gln
XM_017029603.1:c.7241C>A	XP_016885092.1:p.Pro2414Gln
XM_017029604.2:c.7208C>A	XP_016885093.1:p.Pro2403Gln
XM_017029605.1:c.7205C>A	XP_016885094.1:p.Pro2402Gln
XM_017029606.2:c.7178C>A	XP_016885095.1:p.Pro2393Gln
XM_017029607.2:c.7175C>A	XP_016885096.1:p.Pro2392Gln
XM_017029608.2:c.7127C>A	XP_016885097.1:p.Pro2376Gln
XM_017029609.1:c.7091C>A	XP_016885098.1:p.Pro2364Gln
XM_017029610.1:c.7088C>A	XP_016885099.1:p.Pro2363Gln
XM_017029611.1:c.7043C>A	XP_016885100.1:p.Pro2348Gln
XR_001755700.2:n.7708C>A
NM_138270.4:c.7295C>A	NP_612114.2:p.Pro2432Gln
NM_000489.6:c.7409C>A MANE Select	NP_000480.3:p.Pro2470Gln
NM_138270.5:c.7295C>A	NP_612114.2:p.Pro2432Gln