Canonical Allele Identifier: CA878454945

Gene: ATRX

Linked Data

• dbSNP Id: rs1231333742
• gnomAD v3: X-77520726-CTTA-C
• gnomAD v4: X-77520726-CTTA-C
• MyVariant Identifiers: chrX:g.77520727_77520729del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77520731_77520733del , CM000685.2:g.77520731_77520733del	GRCh38
NC_000023.10:g.76776209_76776211del , CM000685.1:g.76776209_76776211del	GRCh37
NC_000023.9:g.76662865_76662867del	NCBI36
NG_008838.2:g.270493_270495del
NG_008838.3:g.270541_270543del

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.7200+59_7200+61del MANE Select	ENSP00000362441.4:n.7200+59_7200+61del
ENST00000675732.1:c.2298+59_2298+61del	ENSP00000502598.1:n.2298+59_2298+61del
ENST00000373344.9:c.7200+59_7200+61del	ENSP00000362441.4:n.7200+59_7200+61del
ENST00000395603.7:c.7086+59_7086+61del	ENSP00000378967.3:n.7086+59_7086+61del
ENST00000480283.5:c.*6828+59_*6828+61del	ENSP00000480196.1:n.*6828+59_*6828+61del
ENST00000623706.3:n.5520+59_5520+61del
ENST00000624766.1:n.431+59_431+61del
NM_000489.4:c.7200+59_7200+61del	NP_000480.3:n.7200+59_7200+61del
NM_138270.3:c.7086+59_7086+61del	NP_612114.2:n.7086+59_7086+61del
XM_005262153.3:c.7197+59_7197+61del	XP_005262210.2:n.7197+59_7197+61del
XM_005262154.3:c.7113+59_7113+61del	XP_005262211.2:n.7113+59_7113+61del
XM_005262155.3:c.7083+59_7083+61del	XP_005262212.2:n.7083+59_7083+61del
XM_005262156.3:c.7035+59_7035+61del	XP_005262213.2:n.7035+59_7035+61del
XM_005262157.3:c.6996+59_6996+61del	XP_005262214.2:n.6996+59_6996+61del
XM_006724666.2:c.7083+59_7083+61del	XP_006724729.1:n.7083+59_7083+61del
XM_006724667.2:c.6921+59_6921+61del	XP_006724730.1:n.6921+59_6921+61del
XR_938400.1:n.8792+59_8792+61del
NM_000489.5:c.7200+59_7200+61del	NP_000480.3:n.7200+59_7200+61del
XM_005262153.5:c.7197+59_7197+61del	XP_005262210.2:n.7197+59_7197+61del
XM_005262154.5:c.7113+59_7113+61del	XP_005262211.2:n.7113+59_7113+61del
XM_005262155.4:c.7083+59_7083+61del	XP_005262212.2:n.7083+59_7083+61del
XM_005262156.4:c.7035+59_7035+61del	XP_005262213.2:n.7035+59_7035+61del
XM_005262157.5:c.6996+59_6996+61del	XP_005262214.2:n.6996+59_6996+61del
XM_006724666.4:c.7083+59_7083+61del	XP_006724729.1:n.7083+59_7083+61del
XM_006724667.3:c.6921+59_6921+61del	XP_006724730.1:n.6921+59_6921+61del
XM_017029601.2:c.7110+59_7110+61del	XP_016885090.1:n.7110+59_7110+61del
XM_017029602.1:c.7080+59_7080+61del	XP_016885091.1:n.7080+59_7080+61del
XM_017029603.1:c.7032+59_7032+61del	XP_016885092.1:n.7032+59_7032+61del
XM_017029604.2:c.6999+59_6999+61del	XP_016885093.1:n.6999+59_6999+61del
XM_017029605.1:c.6996+59_6996+61del	XP_016885094.1:n.6996+59_6996+61del
XM_017029606.2:c.6969+59_6969+61del	XP_016885095.1:n.6969+59_6969+61del
XM_017029607.2:c.6966+59_6966+61del	XP_016885096.1:n.6966+59_6966+61del
XM_017029608.2:c.6918+59_6918+61del	XP_016885097.1:n.6918+59_6918+61del
XM_017029609.1:c.6882+59_6882+61del	XP_016885098.1:n.6882+59_6882+61del
XM_017029610.1:c.6879+59_6879+61del	XP_016885099.1:n.6879+59_6879+61del
XM_017029611.1:c.6834+59_6834+61del	XP_016885100.1:n.6834+59_6834+61del
XR_001755700.2:n.7499+59_7499+61del
NM_138270.4:c.7086+59_7086+61del	NP_612114.2:n.7086+59_7086+61del
NM_000489.6:c.7200+59_7200+61del MANE Select	NP_000480.3:n.7200+59_7200+61del
NM_138270.5:c.7086+59_7086+61del	NP_612114.2:n.7086+59_7086+61del