Canonical Allele Identifier: CA413707658

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907606C>A (hg19) ; chrX:g.77652116C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652116C>A , CM000685.2:g.77652116C>A	GRCh38
NC_000023.10:g.76907606C>A , CM000685.1:g.76907606C>A	GRCh37
NC_000023.9:g.76794262C>A	NCBI36
NG_008838.2:g.139106G>T
NG_008838.3:g.139154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4555G>T MANE Select	ENSP00000362441.4:p.Glu1519Ter
ENST00000373344.9:c.4555G>T	ENSP00000362441.4:p.Glu1519Ter
ENST00000395603.7:c.4441G>T	ENSP00000378967.3:p.Glu1481Ter
ENST00000460639.2:n.35G>T
ENST00000480283.5:c.*4183G>T	ENSP00000480196.1:n.*4183G>T
ENST00000623242.3:c.161G>T
NM_000489.4:c.4555G>T	NP_000480.3:p.Glu1519Ter
NM_138270.3:c.4441G>T	NP_612114.2:p.Glu1481Ter
XM_005262153.3:c.4552G>T	XP_005262210.2:p.Glu1518Ter
XM_005262154.3:c.4468G>T	XP_005262211.2:p.Glu1490Ter
XM_005262155.3:c.4438G>T	XP_005262212.2:p.Glu1480Ter
XM_005262156.3:c.4390G>T	XP_005262213.2:p.Glu1464Ter
XM_005262157.3:c.4351G>T	XP_005262214.2:p.Glu1451Ter
XM_006724666.2:c.4438G>T	XP_006724729.1:p.Glu1480Ter
XM_006724667.2:c.4276G>T	XP_006724730.1:p.Glu1426Ter
XM_006724668.2:c.4555G>T	XP_006724731.1:p.Glu1519Ter
XR_938400.1:n.4823G>T
NM_000489.5:c.4555G>T	NP_000480.3:p.Glu1519Ter
XM_005262153.5:c.4552G>T	XP_005262210.2:p.Glu1518Ter
XM_005262154.5:c.4468G>T	XP_005262211.2:p.Glu1490Ter
XM_005262155.4:c.4438G>T	XP_005262212.2:p.Glu1480Ter
XM_005262156.4:c.4390G>T	XP_005262213.2:p.Glu1464Ter
XM_005262157.5:c.4351G>T	XP_005262214.2:p.Glu1451Ter
XM_006724666.4:c.4438G>T	XP_006724729.1:p.Glu1480Ter
XM_006724667.3:c.4276G>T	XP_006724730.1:p.Glu1426Ter
XM_006724668.3:c.4555G>T	XP_006724731.1:p.Glu1519Ter
XM_017029601.2:c.4465G>T	XP_016885090.1:p.Glu1489Ter
XM_017029602.1:c.4435G>T	XP_016885091.1:p.Glu1479Ter
XM_017029603.1:c.4387G>T	XP_016885092.1:p.Glu1463Ter
XM_017029604.2:c.4354G>T	XP_016885093.1:p.Glu1452Ter
XM_017029605.1:c.4351G>T	XP_016885094.1:p.Glu1451Ter
XM_017029606.2:c.4324G>T	XP_016885095.1:p.Glu1442Ter
XM_017029607.2:c.4321G>T	XP_016885096.1:p.Glu1441Ter
XM_017029608.2:c.4273G>T	XP_016885097.1:p.Glu1425Ter
XM_017029609.1:c.4237G>T	XP_016885098.1:p.Glu1413Ter
XM_017029610.1:c.4234G>T	XP_016885099.1:p.Glu1412Ter
XM_017029611.1:c.4189G>T	XP_016885100.1:p.Glu1397Ter
XR_001755700.2:n.4780G>T
NM_138270.4:c.4441G>T	NP_612114.2:p.Glu1481Ter
NM_000489.6:c.4555G>T MANE Select	NP_000480.3:p.Glu1519Ter
NM_138270.5:c.4441G>T	NP_612114.2:p.Glu1481Ter