Canonical Allele Identifier: CA517471133

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907619T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652129T>G , CM000685.2:g.77652129T>G	GRCh38
NC_000023.10:g.76907619T>G , CM000685.1:g.76907619T>G	GRCh37
NC_000023.9:g.76794275T>G	NCBI36
NG_008838.2:g.139093A>C
NG_008838.3:g.139141A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4542A>C MANE Select	ENSP00000362441.4:p.Arg1514=
ENST00000373344.9:c.4542A>C	ENSP00000362441.4:p.Arg1514=
ENST00000395603.7:c.4428A>C	ENSP00000378967.3:p.Arg1476=
ENST00000460639.2:n.22A>C
ENST00000480283.5:c.*4170A>C	ENSP00000480196.1:n.*4170A>C
ENST00000623242.3:c.148A>C
NM_000489.4:c.4542A>C	NP_000480.3:p.Arg1514=
NM_138270.3:c.4428A>C	NP_612114.2:p.Arg1476=
XM_005262153.3:c.4539A>C	XP_005262210.2:p.Arg1513=
XM_005262154.3:c.4455A>C	XP_005262211.2:p.Arg1485=
XM_005262155.3:c.4425A>C	XP_005262212.2:p.Arg1475=
XM_005262156.3:c.4377A>C	XP_005262213.2:p.Arg1459=
XM_005262157.3:c.4338A>C	XP_005262214.2:p.Arg1446=
XM_006724666.2:c.4425A>C	XP_006724729.1:p.Arg1475=
XM_006724667.2:c.4263A>C	XP_006724730.1:p.Arg1421=
XM_006724668.2:c.4542A>C	XP_006724731.1:p.Arg1514=
XR_938400.1:n.4810A>C
NM_000489.5:c.4542A>C	NP_000480.3:p.Arg1514=
XM_005262153.5:c.4539A>C	XP_005262210.2:p.Arg1513=
XM_005262154.5:c.4455A>C	XP_005262211.2:p.Arg1485=
XM_005262155.4:c.4425A>C	XP_005262212.2:p.Arg1475=
XM_005262156.4:c.4377A>C	XP_005262213.2:p.Arg1459=
XM_005262157.5:c.4338A>C	XP_005262214.2:p.Arg1446=
XM_006724666.4:c.4425A>C	XP_006724729.1:p.Arg1475=
XM_006724667.3:c.4263A>C	XP_006724730.1:p.Arg1421=
XM_006724668.3:c.4542A>C	XP_006724731.1:p.Arg1514=
XM_017029601.2:c.4452A>C	XP_016885090.1:p.Arg1484=
XM_017029602.1:c.4422A>C	XP_016885091.1:p.Arg1474=
XM_017029603.1:c.4374A>C	XP_016885092.1:p.Arg1458=
XM_017029604.2:c.4341A>C	XP_016885093.1:p.Arg1447=
XM_017029605.1:c.4338A>C	XP_016885094.1:p.Arg1446=
XM_017029606.2:c.4311A>C	XP_016885095.1:p.Arg1437=
XM_017029607.2:c.4308A>C	XP_016885096.1:p.Arg1436=
XM_017029608.2:c.4260A>C	XP_016885097.1:p.Arg1420=
XM_017029609.1:c.4224A>C	XP_016885098.1:p.Arg1408=
XM_017029610.1:c.4221A>C	XP_016885099.1:p.Arg1407=
XM_017029611.1:c.4176A>C	XP_016885100.1:p.Arg1392=
XR_001755700.2:n.4767A>C
NM_138270.4:c.4428A>C	NP_612114.2:p.Arg1476=
NM_000489.6:c.4542A>C MANE Select	NP_000480.3:p.Arg1514=
NM_138270.5:c.4428A>C	NP_612114.2:p.Arg1476=