Canonical Allele Identifier: CA413708720

Gene: ATRX

Linked Data

• dbSNP Id: rs2148439454
• MyVariant Identifiers: chrX:g.76907789C>A (hg19) ; chrX:g.77652299C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652299C>A , CM000685.2:g.77652299C>A	GRCh38
NC_000023.10:g.76907789C>A , CM000685.1:g.76907789C>A	GRCh37
NC_000023.9:g.76794445C>A	NCBI36
NG_008838.2:g.138923G>T
NG_008838.3:g.138971G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4372G>T MANE Select	ENSP00000362441.4:p.Glu1458Ter
ENST00000373344.9:c.4372G>T	ENSP00000362441.4:p.Glu1458Ter
ENST00000395603.7:c.4258G>T	ENSP00000378967.3:p.Glu1420Ter
ENST00000480283.5:c.*4000G>T	ENSP00000480196.1:n.*4000G>T
NM_000489.4:c.4372G>T	NP_000480.3:p.Glu1458Ter
NM_138270.3:c.4258G>T	NP_612114.2:p.Glu1420Ter
XM_005262153.3:c.4369G>T	XP_005262210.2:p.Glu1457Ter
XM_005262154.3:c.4285G>T	XP_005262211.2:p.Glu1429Ter
XM_005262155.3:c.4255G>T	XP_005262212.2:p.Glu1419Ter
XM_005262156.3:c.4207G>T	XP_005262213.2:p.Glu1403Ter
XM_005262157.3:c.4168G>T	XP_005262214.2:p.Glu1390Ter
XM_006724666.2:c.4255G>T	XP_006724729.1:p.Glu1419Ter
XM_006724667.2:c.4093G>T	XP_006724730.1:p.Glu1365Ter
XM_006724668.2:c.4372G>T	XP_006724731.1:p.Glu1458Ter
XR_938400.1:n.4640G>T
NM_000489.5:c.4372G>T	NP_000480.3:p.Glu1458Ter
XM_005262153.5:c.4369G>T	XP_005262210.2:p.Glu1457Ter
XM_005262154.5:c.4285G>T	XP_005262211.2:p.Glu1429Ter
XM_005262155.4:c.4255G>T	XP_005262212.2:p.Glu1419Ter
XM_005262156.4:c.4207G>T	XP_005262213.2:p.Glu1403Ter
XM_005262157.5:c.4168G>T	XP_005262214.2:p.Glu1390Ter
XM_006724666.4:c.4255G>T	XP_006724729.1:p.Glu1419Ter
XM_006724667.3:c.4093G>T	XP_006724730.1:p.Glu1365Ter
XM_006724668.3:c.4372G>T	XP_006724731.1:p.Glu1458Ter
XM_017029601.2:c.4282G>T	XP_016885090.1:p.Glu1428Ter
XM_017029602.1:c.4252G>T	XP_016885091.1:p.Glu1418Ter
XM_017029603.1:c.4204G>T	XP_016885092.1:p.Glu1402Ter
XM_017029604.2:c.4171G>T	XP_016885093.1:p.Glu1391Ter
XM_017029605.1:c.4168G>T	XP_016885094.1:p.Glu1390Ter
XM_017029606.2:c.4141G>T	XP_016885095.1:p.Glu1381Ter
XM_017029607.2:c.4138G>T	XP_016885096.1:p.Glu1380Ter
XM_017029608.2:c.4090G>T	XP_016885097.1:p.Glu1364Ter
XM_017029609.1:c.4054G>T	XP_016885098.1:p.Glu1352Ter
XM_017029610.1:c.4051G>T	XP_016885099.1:p.Glu1351Ter
XM_017029611.1:c.4006G>T	XP_016885100.1:p.Glu1336Ter
XR_001755700.2:n.4597G>T
NM_138270.4:c.4258G>T	NP_612114.2:p.Glu1420Ter
NM_000489.6:c.4372G>T MANE Select	NP_000480.3:p.Glu1458Ter
NM_138270.5:c.4258G>T	NP_612114.2:p.Glu1420Ter