Canonical Allele Identifier: CA413704607

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764005G>C (hg19) ; chrX:g.77508527G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508527G>C , CM000685.2:g.77508527G>C	GRCh38
NC_000023.10:g.76764005G>C , CM000685.1:g.76764005G>C	GRCh37
NC_000023.9:g.76650661G>C	NCBI36
NG_008838.2:g.282695C>G
NG_008838.3:g.282743C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7303C>G MANE Select	ENSP00000362441.4:p.His2435Asp
ENST00000675732.1:c.2401C>G	ENSP00000502598.1:p.His801Asp
ENST00000373344.9:c.7303C>G	ENSP00000362441.4:p.His2435Asp
ENST00000395603.7:c.7189C>G	ENSP00000378967.3:p.His2397Asp
ENST00000480283.5:c.*6931C>G	ENSP00000480196.1:n.*6931C>G
ENST00000623706.3:n.5623C>G
ENST00000624766.1:n.534C>G
NM_000489.4:c.7303C>G	NP_000480.3:p.His2435Asp
NM_138270.3:c.7189C>G	NP_612114.2:p.His2397Asp
XM_005262153.3:c.7300C>G	XP_005262210.2:p.His2434Asp
XM_005262154.3:c.7216C>G	XP_005262211.2:p.His2406Asp
XM_005262155.3:c.7186C>G	XP_005262212.2:p.His2396Asp
XM_005262156.3:c.7138C>G	XP_005262213.2:p.His2380Asp
XM_005262157.3:c.7099C>G	XP_005262214.2:p.His2367Asp
XM_006724666.2:c.7186C>G	XP_006724729.1:p.His2396Asp
XM_006724667.2:c.7024C>G	XP_006724730.1:p.His2342Asp
XR_938400.1:n.8895C>G
NM_000489.5:c.7303C>G	NP_000480.3:p.His2435Asp
XM_005262153.5:c.7300C>G	XP_005262210.2:p.His2434Asp
XM_005262154.5:c.7216C>G	XP_005262211.2:p.His2406Asp
XM_005262155.4:c.7186C>G	XP_005262212.2:p.His2396Asp
XM_005262156.4:c.7138C>G	XP_005262213.2:p.His2380Asp
XM_005262157.5:c.7099C>G	XP_005262214.2:p.His2367Asp
XM_006724666.4:c.7186C>G	XP_006724729.1:p.His2396Asp
XM_006724667.3:c.7024C>G	XP_006724730.1:p.His2342Asp
XM_017029601.2:c.7213C>G	XP_016885090.1:p.His2405Asp
XM_017029602.1:c.7183C>G	XP_016885091.1:p.His2395Asp
XM_017029603.1:c.7135C>G	XP_016885092.1:p.His2379Asp
XM_017029604.2:c.7102C>G	XP_016885093.1:p.His2368Asp
XM_017029605.1:c.7099C>G	XP_016885094.1:p.His2367Asp
XM_017029606.2:c.7072C>G	XP_016885095.1:p.His2358Asp
XM_017029607.2:c.7069C>G	XP_016885096.1:p.His2357Asp
XM_017029608.2:c.7021C>G	XP_016885097.1:p.His2341Asp
XM_017029609.1:c.6985C>G	XP_016885098.1:p.His2329Asp
XM_017029610.1:c.6982C>G	XP_016885099.1:p.His2328Asp
XM_017029611.1:c.6937C>G	XP_016885100.1:p.His2313Asp
XR_001755700.2:n.7602C>G
NM_138270.4:c.7189C>G	NP_612114.2:p.His2397Asp
NM_000489.6:c.7303C>G MANE Select	NP_000480.3:p.His2435Asp
NM_138270.5:c.7189C>G	NP_612114.2:p.His2397Asp