Canonical Allele Identifier: CA517374148

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764006A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508528A>G , CM000685.2:g.77508528A>G	GRCh38
NC_000023.10:g.76764006A>G , CM000685.1:g.76764006A>G	GRCh37
NC_000023.9:g.76650662A>G	NCBI36
NG_008838.2:g.282694T>C
NG_008838.3:g.282742T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7302T>C MANE Select	ENSP00000362441.4:p.Gly2434=
ENST00000675732.1:c.2400T>C	ENSP00000502598.1:p.Gly800=
ENST00000373344.9:c.7302T>C	ENSP00000362441.4:p.Gly2434=
ENST00000395603.7:c.7188T>C	ENSP00000378967.3:p.Gly2396=
ENST00000480283.5:c.*6930T>C	ENSP00000480196.1:n.*6930T>C
ENST00000623706.3:n.5622T>C
ENST00000624766.1:n.533T>C
NM_000489.4:c.7302T>C	NP_000480.3:p.Gly2434=
NM_138270.3:c.7188T>C	NP_612114.2:p.Gly2396=
XM_005262153.3:c.7299T>C	XP_005262210.2:p.Gly2433=
XM_005262154.3:c.7215T>C	XP_005262211.2:p.Gly2405=
XM_005262155.3:c.7185T>C	XP_005262212.2:p.Gly2395=
XM_005262156.3:c.7137T>C	XP_005262213.2:p.Gly2379=
XM_005262157.3:c.7098T>C	XP_005262214.2:p.Gly2366=
XM_006724666.2:c.7185T>C	XP_006724729.1:p.Gly2395=
XM_006724667.2:c.7023T>C	XP_006724730.1:p.Gly2341=
XR_938400.1:n.8894T>C
NM_000489.5:c.7302T>C	NP_000480.3:p.Gly2434=
XM_005262153.5:c.7299T>C	XP_005262210.2:p.Gly2433=
XM_005262154.5:c.7215T>C	XP_005262211.2:p.Gly2405=
XM_005262155.4:c.7185T>C	XP_005262212.2:p.Gly2395=
XM_005262156.4:c.7137T>C	XP_005262213.2:p.Gly2379=
XM_005262157.5:c.7098T>C	XP_005262214.2:p.Gly2366=
XM_006724666.4:c.7185T>C	XP_006724729.1:p.Gly2395=
XM_006724667.3:c.7023T>C	XP_006724730.1:p.Gly2341=
XM_017029601.2:c.7212T>C	XP_016885090.1:p.Gly2404=
XM_017029602.1:c.7182T>C	XP_016885091.1:p.Gly2394=
XM_017029603.1:c.7134T>C	XP_016885092.1:p.Gly2378=
XM_017029604.2:c.7101T>C	XP_016885093.1:p.Gly2367=
XM_017029605.1:c.7098T>C	XP_016885094.1:p.Gly2366=
XM_017029606.2:c.7071T>C	XP_016885095.1:p.Gly2357=
XM_017029607.2:c.7068T>C	XP_016885096.1:p.Gly2356=
XM_017029608.2:c.7020T>C	XP_016885097.1:p.Gly2340=
XM_017029609.1:c.6984T>C	XP_016885098.1:p.Gly2328=
XM_017029610.1:c.6981T>C	XP_016885099.1:p.Gly2327=
XM_017029611.1:c.6936T>C	XP_016885100.1:p.Gly2312=
XR_001755700.2:n.7601T>C
NM_138270.4:c.7188T>C	NP_612114.2:p.Gly2396=
NM_000489.6:c.7302T>C MANE Select	NP_000480.3:p.Gly2434=
NM_138270.5:c.7188T>C	NP_612114.2:p.Gly2396=