Canonical Allele Identifier: CA517471214

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907654T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652164T>G , CM000685.2:g.77652164T>G	GRCh38
NC_000023.10:g.76907654T>G , CM000685.1:g.76907654T>G	GRCh37
NC_000023.9:g.76794310T>G	NCBI36
NG_008838.2:g.139058A>C
NG_008838.3:g.139106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4507A>C MANE Select	ENSP00000362441.4:p.Arg1503=
ENST00000373344.9:c.4507A>C	ENSP00000362441.4:p.Arg1503=
ENST00000395603.7:c.4393A>C	ENSP00000378967.3:p.Arg1465=
ENST00000480283.5:c.*4135A>C	ENSP00000480196.1:n.*4135A>C
ENST00000623242.3:c.113A>C
NM_000489.4:c.4507A>C	NP_000480.3:p.Arg1503=
NM_138270.3:c.4393A>C	NP_612114.2:p.Arg1465=
XM_005262153.3:c.4504A>C	XP_005262210.2:p.Arg1502=
XM_005262154.3:c.4420A>C	XP_005262211.2:p.Arg1474=
XM_005262155.3:c.4390A>C	XP_005262212.2:p.Arg1464=
XM_005262156.3:c.4342A>C	XP_005262213.2:p.Arg1448=
XM_005262157.3:c.4303A>C	XP_005262214.2:p.Arg1435=
XM_006724666.2:c.4390A>C	XP_006724729.1:p.Arg1464=
XM_006724667.2:c.4228A>C	XP_006724730.1:p.Arg1410=
XM_006724668.2:c.4507A>C	XP_006724731.1:p.Arg1503=
XR_938400.1:n.4775A>C
NM_000489.5:c.4507A>C	NP_000480.3:p.Arg1503=
XM_005262153.5:c.4504A>C	XP_005262210.2:p.Arg1502=
XM_005262154.5:c.4420A>C	XP_005262211.2:p.Arg1474=
XM_005262155.4:c.4390A>C	XP_005262212.2:p.Arg1464=
XM_005262156.4:c.4342A>C	XP_005262213.2:p.Arg1448=
XM_005262157.5:c.4303A>C	XP_005262214.2:p.Arg1435=
XM_006724666.4:c.4390A>C	XP_006724729.1:p.Arg1464=
XM_006724667.3:c.4228A>C	XP_006724730.1:p.Arg1410=
XM_006724668.3:c.4507A>C	XP_006724731.1:p.Arg1503=
XM_017029601.2:c.4417A>C	XP_016885090.1:p.Arg1473=
XM_017029602.1:c.4387A>C	XP_016885091.1:p.Arg1463=
XM_017029603.1:c.4339A>C	XP_016885092.1:p.Arg1447=
XM_017029604.2:c.4306A>C	XP_016885093.1:p.Arg1436=
XM_017029605.1:c.4303A>C	XP_016885094.1:p.Arg1435=
XM_017029606.2:c.4276A>C	XP_016885095.1:p.Arg1426=
XM_017029607.2:c.4273A>C	XP_016885096.1:p.Arg1425=
XM_017029608.2:c.4225A>C	XP_016885097.1:p.Arg1409=
XM_017029609.1:c.4189A>C	XP_016885098.1:p.Arg1397=
XM_017029610.1:c.4186A>C	XP_016885099.1:p.Arg1396=
XM_017029611.1:c.4141A>C	XP_016885100.1:p.Arg1381=
XR_001755700.2:n.4732A>C
NM_138270.4:c.4393A>C	NP_612114.2:p.Arg1465=
NM_000489.6:c.4507A>C MANE Select	NP_000480.3:p.Arg1503=
NM_138270.5:c.4393A>C	NP_612114.2:p.Arg1465=