Canonical Allele Identifier: CA331560028

Gene: ATRX

Linked Data

• dbSNP Id: rs782268822
• gnomAD v2: X-76763778-AT-A
• gnomAD v4: X-77508300-AT-A
• MyVariant Identifiers: chrX:g.76763779del (hg19) ; chrX:g.77508301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508301del , CM000685.2:g.77508301del	GRCh38
NC_000023.10:g.76763779del , CM000685.1:g.76763779del	GRCh37
NC_000023.9:g.76650435del	NCBI36
NG_008838.2:g.282921del
NG_008838.3:g.282969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.*50del MANE Select	ENSP00000362441.4:n.*50del
ENST00000675732.1:c.*50del	ENSP00000502598.1:n.*50del
ENST00000373344.9:c.*50del	ENSP00000362441.4:n.*50del
ENST00000395603.7:c.*50del	ENSP00000378967.3:n.*50del
ENST00000480283.5:c.*7157del	ENSP00000480196.1:n.*7157del
ENST00000623706.3:n.5849del
NM_000489.4:c.*50del	NP_000480.3:n.*50del
NM_138270.3:c.*50del	NP_612114.2:n.*50del
XM_005262153.3:c.*50del	XP_005262210.2:n.*50del
XM_005262154.3:c.*50del	XP_005262211.2:n.*50del
XM_005262155.3:c.*50del	XP_005262212.2:n.*50del
XM_005262156.3:c.*50del	XP_005262213.2:n.*50del
XM_005262157.3:c.*50del	XP_005262214.2:n.*50del
XM_006724666.2:c.*50del	XP_006724729.1:n.*50del
XM_006724667.2:c.*50del	XP_006724730.1:n.*50del
XR_938400.1:n.9121del
NM_000489.5:c.*50del	NP_000480.3:n.*50del
XM_005262153.5:c.*50del	XP_005262210.2:n.*50del
XM_005262154.5:c.*50del	XP_005262211.2:n.*50del
XM_005262155.4:c.*50del	XP_005262212.2:n.*50del
XM_005262156.4:c.*50del	XP_005262213.2:n.*50del
XM_005262157.5:c.*50del	XP_005262214.2:n.*50del
XM_006724666.4:c.*50del	XP_006724729.1:n.*50del
XM_006724667.3:c.*50del	XP_006724730.1:n.*50del
XM_017029601.2:c.*50del	XP_016885090.1:n.*50del
XM_017029602.1:c.*50del	XP_016885091.1:n.*50del
XM_017029603.1:c.*50del	XP_016885092.1:n.*50del
XM_017029604.2:c.*50del	XP_016885093.1:n.*50del
XM_017029605.1:c.*50del	XP_016885094.1:n.*50del
XM_017029606.2:c.*50del	XP_016885095.1:n.*50del
XM_017029607.2:c.*50del	XP_016885096.1:n.*50del
XM_017029608.2:c.*50del	XP_016885097.1:n.*50del
XM_017029609.1:c.*50del	XP_016885098.1:n.*50del
XM_017029610.1:c.*50del	XP_016885099.1:n.*50del
XM_017029611.1:c.*50del	XP_016885100.1:n.*50del
XR_001755700.2:n.7828del
NM_138270.4:c.*50del	NP_612114.2:n.*50del
NM_000489.6:c.*50del MANE Select	NP_000480.3:n.*50del
NM_138270.5:c.*50del	NP_612114.2:n.*50del