Canonical Allele Identifier: CA413704510

Gene: ATRX

Linked Data

• dbSNP Id: rs2147650028
• MyVariant Identifiers: chrX:g.76763993G>A (hg19) ; chrX:g.77508515G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508515G>A , CM000685.2:g.77508515G>A	GRCh38
NC_000023.10:g.76763993G>A , CM000685.1:g.76763993G>A	GRCh37
NC_000023.9:g.76650649G>A	NCBI36
NG_008838.2:g.282707C>T
NG_008838.3:g.282755C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7315C>T MANE Select	ENSP00000362441.4:p.Pro2439Ser
ENST00000675732.1:c.2413C>T	ENSP00000502598.1:p.Pro805Ser
ENST00000373344.9:c.7315C>T	ENSP00000362441.4:p.Pro2439Ser
ENST00000395603.7:c.7201C>T	ENSP00000378967.3:p.Pro2401Ser
ENST00000480283.5:c.*6943C>T	ENSP00000480196.1:n.*6943C>T
ENST00000623706.3:n.5635C>T
ENST00000624766.1:n.546C>T
NM_000489.4:c.7315C>T	NP_000480.3:p.Pro2439Ser
NM_138270.3:c.7201C>T	NP_612114.2:p.Pro2401Ser
XM_005262153.3:c.7312C>T	XP_005262210.2:p.Pro2438Ser
XM_005262154.3:c.7228C>T	XP_005262211.2:p.Pro2410Ser
XM_005262155.3:c.7198C>T	XP_005262212.2:p.Pro2400Ser
XM_005262156.3:c.7150C>T	XP_005262213.2:p.Pro2384Ser
XM_005262157.3:c.7111C>T	XP_005262214.2:p.Pro2371Ser
XM_006724666.2:c.7198C>T	XP_006724729.1:p.Pro2400Ser
XM_006724667.2:c.7036C>T	XP_006724730.1:p.Pro2346Ser
XR_938400.1:n.8907C>T
NM_000489.5:c.7315C>T	NP_000480.3:p.Pro2439Ser
XM_005262153.5:c.7312C>T	XP_005262210.2:p.Pro2438Ser
XM_005262154.5:c.7228C>T	XP_005262211.2:p.Pro2410Ser
XM_005262155.4:c.7198C>T	XP_005262212.2:p.Pro2400Ser
XM_005262156.4:c.7150C>T	XP_005262213.2:p.Pro2384Ser
XM_005262157.5:c.7111C>T	XP_005262214.2:p.Pro2371Ser
XM_006724666.4:c.7198C>T	XP_006724729.1:p.Pro2400Ser
XM_006724667.3:c.7036C>T	XP_006724730.1:p.Pro2346Ser
XM_017029601.2:c.7225C>T	XP_016885090.1:p.Pro2409Ser
XM_017029602.1:c.7195C>T	XP_016885091.1:p.Pro2399Ser
XM_017029603.1:c.7147C>T	XP_016885092.1:p.Pro2383Ser
XM_017029604.2:c.7114C>T	XP_016885093.1:p.Pro2372Ser
XM_017029605.1:c.7111C>T	XP_016885094.1:p.Pro2371Ser
XM_017029606.2:c.7084C>T	XP_016885095.1:p.Pro2362Ser
XM_017029607.2:c.7081C>T	XP_016885096.1:p.Pro2361Ser
XM_017029608.2:c.7033C>T	XP_016885097.1:p.Pro2345Ser
XM_017029609.1:c.6997C>T	XP_016885098.1:p.Pro2333Ser
XM_017029610.1:c.6994C>T	XP_016885099.1:p.Pro2332Ser
XM_017029611.1:c.6949C>T	XP_016885100.1:p.Pro2317Ser
XR_001755700.2:n.7614C>T
NM_138270.4:c.7201C>T	NP_612114.2:p.Pro2401Ser
NM_000489.6:c.7315C>T MANE Select	NP_000480.3:p.Pro2439Ser
NM_138270.5:c.7201C>T	NP_612114.2:p.Pro2401Ser