Canonical Allele Identifier: CA517471458

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907706T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652216T>C , CM000685.2:g.77652216T>C	GRCh38
NC_000023.10:g.76907706T>C , CM000685.1:g.76907706T>C	GRCh37
NC_000023.9:g.76794362T>C	NCBI36
NG_008838.2:g.139006A>G
NG_008838.3:g.139054A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4455A>G MANE Select	ENSP00000362441.4:p.Lys1485=
ENST00000373344.9:c.4455A>G	ENSP00000362441.4:p.Lys1485=
ENST00000395603.7:c.4341A>G	ENSP00000378967.3:p.Lys1447=
ENST00000480283.5:c.*4083A>G	ENSP00000480196.1:n.*4083A>G
ENST00000623242.3:c.61A>G
NM_000489.4:c.4455A>G	NP_000480.3:p.Lys1485=
NM_138270.3:c.4341A>G	NP_612114.2:p.Lys1447=
XM_005262153.3:c.4452A>G	XP_005262210.2:p.Lys1484=
XM_005262154.3:c.4368A>G	XP_005262211.2:p.Lys1456=
XM_005262155.3:c.4338A>G	XP_005262212.2:p.Lys1446=
XM_005262156.3:c.4290A>G	XP_005262213.2:p.Lys1430=
XM_005262157.3:c.4251A>G	XP_005262214.2:p.Lys1417=
XM_006724666.2:c.4338A>G	XP_006724729.1:p.Lys1446=
XM_006724667.2:c.4176A>G	XP_006724730.1:p.Lys1392=
XM_006724668.2:c.4455A>G	XP_006724731.1:p.Lys1485=
XR_938400.1:n.4723A>G
NM_000489.5:c.4455A>G	NP_000480.3:p.Lys1485=
XM_005262153.5:c.4452A>G	XP_005262210.2:p.Lys1484=
XM_005262154.5:c.4368A>G	XP_005262211.2:p.Lys1456=
XM_005262155.4:c.4338A>G	XP_005262212.2:p.Lys1446=
XM_005262156.4:c.4290A>G	XP_005262213.2:p.Lys1430=
XM_005262157.5:c.4251A>G	XP_005262214.2:p.Lys1417=
XM_006724666.4:c.4338A>G	XP_006724729.1:p.Lys1446=
XM_006724667.3:c.4176A>G	XP_006724730.1:p.Lys1392=
XM_006724668.3:c.4455A>G	XP_006724731.1:p.Lys1485=
XM_017029601.2:c.4365A>G	XP_016885090.1:p.Lys1455=
XM_017029602.1:c.4335A>G	XP_016885091.1:p.Lys1445=
XM_017029603.1:c.4287A>G	XP_016885092.1:p.Lys1429=
XM_017029604.2:c.4254A>G	XP_016885093.1:p.Lys1418=
XM_017029605.1:c.4251A>G	XP_016885094.1:p.Lys1417=
XM_017029606.2:c.4224A>G	XP_016885095.1:p.Lys1408=
XM_017029607.2:c.4221A>G	XP_016885096.1:p.Lys1407=
XM_017029608.2:c.4173A>G	XP_016885097.1:p.Lys1391=
XM_017029609.1:c.4137A>G	XP_016885098.1:p.Lys1379=
XM_017029610.1:c.4134A>G	XP_016885099.1:p.Lys1378=
XM_017029611.1:c.4089A>G	XP_016885100.1:p.Lys1363=
XR_001755700.2:n.4680A>G
NM_138270.4:c.4341A>G	NP_612114.2:p.Lys1447=
NM_000489.6:c.4455A>G MANE Select	NP_000480.3:p.Lys1485=
NM_138270.5:c.4341A>G	NP_612114.2:p.Lys1447=