Canonical Allele Identifier: CA517374010

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763886A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508408A>C , CM000685.2:g.77508408A>C	GRCh38
NC_000023.10:g.76763886A>C , CM000685.1:g.76763886A>C	GRCh37
NC_000023.9:g.76650542A>C	NCBI36
NG_008838.2:g.282814T>G
NG_008838.3:g.282862T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7422T>G MANE Select	ENSP00000362441.4:p.Arg2474=
ENST00000675732.1:c.2520T>G	ENSP00000502598.1:p.Arg840=
ENST00000373344.9:c.7422T>G	ENSP00000362441.4:p.Arg2474=
ENST00000395603.7:c.7308T>G	ENSP00000378967.3:p.Arg2436=
ENST00000480283.5:c.*7050T>G	ENSP00000480196.1:n.*7050T>G
ENST00000623706.3:n.5742T>G
NM_000489.4:c.7422T>G	NP_000480.3:p.Arg2474=
NM_138270.3:c.7308T>G	NP_612114.2:p.Arg2436=
XM_005262153.3:c.7419T>G	XP_005262210.2:p.Arg2473=
XM_005262154.3:c.7335T>G	XP_005262211.2:p.Arg2445=
XM_005262155.3:c.7305T>G	XP_005262212.2:p.Arg2435=
XM_005262156.3:c.7257T>G	XP_005262213.2:p.Arg2419=
XM_005262157.3:c.7218T>G	XP_005262214.2:p.Arg2406=
XM_006724666.2:c.7305T>G	XP_006724729.1:p.Arg2435=
XM_006724667.2:c.7143T>G	XP_006724730.1:p.Arg2381=
XR_938400.1:n.9014T>G
NM_000489.5:c.7422T>G	NP_000480.3:p.Arg2474=
XM_005262153.5:c.7419T>G	XP_005262210.2:p.Arg2473=
XM_005262154.5:c.7335T>G	XP_005262211.2:p.Arg2445=
XM_005262155.4:c.7305T>G	XP_005262212.2:p.Arg2435=
XM_005262156.4:c.7257T>G	XP_005262213.2:p.Arg2419=
XM_005262157.5:c.7218T>G	XP_005262214.2:p.Arg2406=
XM_006724666.4:c.7305T>G	XP_006724729.1:p.Arg2435=
XM_006724667.3:c.7143T>G	XP_006724730.1:p.Arg2381=
XM_017029601.2:c.7332T>G	XP_016885090.1:p.Arg2444=
XM_017029602.1:c.7302T>G	XP_016885091.1:p.Arg2434=
XM_017029603.1:c.7254T>G	XP_016885092.1:p.Arg2418=
XM_017029604.2:c.7221T>G	XP_016885093.1:p.Arg2407=
XM_017029605.1:c.7218T>G	XP_016885094.1:p.Arg2406=
XM_017029606.2:c.7191T>G	XP_016885095.1:p.Arg2397=
XM_017029607.2:c.7188T>G	XP_016885096.1:p.Arg2396=
XM_017029608.2:c.7140T>G	XP_016885097.1:p.Arg2380=
XM_017029609.1:c.7104T>G	XP_016885098.1:p.Arg2368=
XM_017029610.1:c.7101T>G	XP_016885099.1:p.Arg2367=
XM_017029611.1:c.7056T>G	XP_016885100.1:p.Arg2352=
XR_001755700.2:n.7721T>G
NM_138270.4:c.7308T>G	NP_612114.2:p.Arg2436=
NM_000489.6:c.7422T>G MANE Select	NP_000480.3:p.Arg2474=
NM_138270.5:c.7308T>G	NP_612114.2:p.Arg2436=