Canonical Allele Identifier: CA878452683

Gene: ATRX

Linked Data

• dbSNP Id: rs1266210721
• gnomAD v4: X-77508307-ATCTT-A
• MyVariant Identifiers: chrX:g.77508308_77508311del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508311_77508314del , CM000685.2:g.77508311_77508314del	GRCh38
NC_000023.10:g.76763789_76763792del , CM000685.1:g.76763789_76763792del	GRCh37
NC_000023.9:g.76650445_76650448del	NCBI36
NG_008838.2:g.282911_282914del
NG_008838.3:g.282959_282962del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.*40_*43del MANE Select	ENSP00000362441.4:n.*40_*43del
ENST00000675732.1:c.*40_*43del	ENSP00000502598.1:n.*40_*43del
ENST00000373344.9:c.*40_*43del	ENSP00000362441.4:n.*40_*43del
ENST00000395603.7:c.*40_*43del	ENSP00000378967.3:n.*40_*43del
ENST00000480283.5:c.*7147_*7150del	ENSP00000480196.1:n.*7147_*7150del
ENST00000623706.3:n.5839_5842del
NM_000489.4:c.*40_*43del	NP_000480.3:n.*40_*43del
NM_138270.3:c.*40_*43del	NP_612114.2:n.*40_*43del
XM_005262153.3:c.*40_*43del	XP_005262210.2:n.*40_*43del
XM_005262154.3:c.*40_*43del	XP_005262211.2:n.*40_*43del
XM_005262155.3:c.*40_*43del	XP_005262212.2:n.*40_*43del
XM_005262156.3:c.*40_*43del	XP_005262213.2:n.*40_*43del
XM_005262157.3:c.*40_*43del	XP_005262214.2:n.*40_*43del
XM_006724666.2:c.*40_*43del	XP_006724729.1:n.*40_*43del
XM_006724667.2:c.*40_*43del	XP_006724730.1:n.*40_*43del
XR_938400.1:n.9111_9114del
NM_000489.5:c.*40_*43del	NP_000480.3:n.*40_*43del
XM_005262153.5:c.*40_*43del	XP_005262210.2:n.*40_*43del
XM_005262154.5:c.*40_*43del	XP_005262211.2:n.*40_*43del
XM_005262155.4:c.*40_*43del	XP_005262212.2:n.*40_*43del
XM_005262156.4:c.*40_*43del	XP_005262213.2:n.*40_*43del
XM_005262157.5:c.*40_*43del	XP_005262214.2:n.*40_*43del
XM_006724666.4:c.*40_*43del	XP_006724729.1:n.*40_*43del
XM_006724667.3:c.*40_*43del	XP_006724730.1:n.*40_*43del
XM_017029601.2:c.*40_*43del	XP_016885090.1:n.*40_*43del
XM_017029602.1:c.*40_*43del	XP_016885091.1:n.*40_*43del
XM_017029603.1:c.*40_*43del	XP_016885092.1:n.*40_*43del
XM_017029604.2:c.*40_*43del	XP_016885093.1:n.*40_*43del
XM_017029605.1:c.*40_*43del	XP_016885094.1:n.*40_*43del
XM_017029606.2:c.*40_*43del	XP_016885095.1:n.*40_*43del
XM_017029607.2:c.*40_*43del	XP_016885096.1:n.*40_*43del
XM_017029608.2:c.*40_*43del	XP_016885097.1:n.*40_*43del
XM_017029609.1:c.*40_*43del	XP_016885098.1:n.*40_*43del
XM_017029610.1:c.*40_*43del	XP_016885099.1:n.*40_*43del
XM_017029611.1:c.*40_*43del	XP_016885100.1:n.*40_*43del
XR_001755700.2:n.7818_7821del
NM_138270.4:c.*40_*43del	NP_612114.2:n.*40_*43del
NM_000489.6:c.*40_*43del MANE Select	NP_000480.3:n.*40_*43del
NM_138270.5:c.*40_*43del	NP_612114.2:n.*40_*43del