Canonical Allele Identifier: CA2738739958

Gene: ATRX

Linked Data

• dbSNP Id: rs2148087805

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77589808del , CM000685.2:g.77589808del	GRCh38
NC_000023.10:g.76845278del , CM000685.1:g.76845278del	GRCh37
NC_000023.9:g.76731934del	NCBI36
NG_008838.2:g.201414del
NG_008838.3:g.201462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6217+26del MANE Select	ENSP00000362441.4:n.6217+26del
ENST00000636868.1:n.39+26del
ENST00000675732.1:c.1315+26del	ENSP00000502598.1:n.1315+26del
ENST00000373344.9:c.6217+26del	ENSP00000362441.4:n.6217+26del
ENST00000395603.7:c.6103+26del	ENSP00000378967.3:n.6103+26del
ENST00000480283.5:c.*5845+26del	ENSP00000480196.1:n.*5845+26del
ENST00000623316.1:c.701+26del
ENST00000623706.3:n.3287+26del
NM_000489.4:c.6217+26del	NP_000480.3:n.6217+26del
NM_138270.3:c.6103+26del	NP_612114.2:n.6103+26del
XM_005262153.3:c.6214+26del	XP_005262210.2:n.6214+26del
XM_005262154.3:c.6130+26del	XP_005262211.2:n.6130+26del
XM_005262155.3:c.6100+26del	XP_005262212.2:n.6100+26del
XM_005262156.3:c.6052+26del	XP_005262213.2:n.6052+26del
XM_005262157.3:c.6013+26del	XP_005262214.2:n.6013+26del
XM_006724666.2:c.6100+26del	XP_006724729.1:n.6100+26del
XM_006724667.2:c.5938+26del	XP_006724730.1:n.5938+26del
XR_938400.1:n.6559+26del
NM_000489.5:c.6217+26del	NP_000480.3:n.6217+26del
XM_005262153.5:c.6214+26del	XP_005262210.2:n.6214+26del
XM_005262154.5:c.6130+26del	XP_005262211.2:n.6130+26del
XM_005262155.4:c.6100+26del	XP_005262212.2:n.6100+26del
XM_005262156.4:c.6052+26del	XP_005262213.2:n.6052+26del
XM_005262157.5:c.6013+26del	XP_005262214.2:n.6013+26del
XM_006724666.4:c.6100+26del	XP_006724729.1:n.6100+26del
XM_006724667.3:c.5938+26del	XP_006724730.1:n.5938+26del
XM_017029601.2:c.6127+26del	XP_016885090.1:n.6127+26del
XM_017029602.1:c.6097+26del	XP_016885091.1:n.6097+26del
XM_017029603.1:c.6049+26del	XP_016885092.1:n.6049+26del
XM_017029604.2:c.6016+26del	XP_016885093.1:n.6016+26del
XM_017029605.1:c.6013+26del	XP_016885094.1:n.6013+26del
XM_017029606.2:c.5986+26del	XP_016885095.1:n.5986+26del
XM_017029607.2:c.5983+26del	XP_016885096.1:n.5983+26del
XM_017029608.2:c.5935+26del	XP_016885097.1:n.5935+26del
XM_017029609.1:c.5899+26del	XP_016885098.1:n.5899+26del
XM_017029610.1:c.5896+26del	XP_016885099.1:n.5896+26del
XM_017029611.1:c.5851+26del	XP_016885100.1:n.5851+26del
XR_001755700.2:n.6516+26del
NM_138270.4:c.6103+26del	NP_612114.2:n.6103+26del
NM_000489.6:c.6217+26del MANE Select	NP_000480.3:n.6217+26del
NM_138270.5:c.6103+26del	NP_612114.2:n.6103+26del