Canonical Allele Identifier: CA2694139276

Gene: ATRX

Linked Data

• gnomAD v4: X-77520730-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77520730T>C , CM000685.2:g.77520730T>C	GRCh38
NC_000023.10:g.76776208T>C , CM000685.1:g.76776208T>C	GRCh37
NC_000023.9:g.76662864T>C	NCBI36
NG_008838.2:g.270492A>G
NG_008838.3:g.270540A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.7200+58A>G MANE Select	ENSP00000362441.4:n.7200+58A>G
ENST00000675732.1:c.2298+58A>G	ENSP00000502598.1:n.2298+58A>G
ENST00000373344.9:c.7200+58A>G	ENSP00000362441.4:n.7200+58A>G
ENST00000395603.7:c.7086+58A>G	ENSP00000378967.3:n.7086+58A>G
ENST00000480283.5:c.*6828+58A>G	ENSP00000480196.1:n.*6828+58A>G
ENST00000623706.3:n.5520+58A>G
ENST00000624766.1:n.431+58A>G
NM_000489.4:c.7200+58A>G	NP_000480.3:n.7200+58A>G
NM_138270.3:c.7086+58A>G	NP_612114.2:n.7086+58A>G
XM_005262153.3:c.7197+58A>G	XP_005262210.2:n.7197+58A>G
XM_005262154.3:c.7113+58A>G	XP_005262211.2:n.7113+58A>G
XM_005262155.3:c.7083+58A>G	XP_005262212.2:n.7083+58A>G
XM_005262156.3:c.7035+58A>G	XP_005262213.2:n.7035+58A>G
XM_005262157.3:c.6996+58A>G	XP_005262214.2:n.6996+58A>G
XM_006724666.2:c.7083+58A>G	XP_006724729.1:n.7083+58A>G
XM_006724667.2:c.6921+58A>G	XP_006724730.1:n.6921+58A>G
XR_938400.1:n.8792+58A>G
NM_000489.5:c.7200+58A>G	NP_000480.3:n.7200+58A>G
XM_005262153.5:c.7197+58A>G	XP_005262210.2:n.7197+58A>G
XM_005262154.5:c.7113+58A>G	XP_005262211.2:n.7113+58A>G
XM_005262155.4:c.7083+58A>G	XP_005262212.2:n.7083+58A>G
XM_005262156.4:c.7035+58A>G	XP_005262213.2:n.7035+58A>G
XM_005262157.5:c.6996+58A>G	XP_005262214.2:n.6996+58A>G
XM_006724666.4:c.7083+58A>G	XP_006724729.1:n.7083+58A>G
XM_006724667.3:c.6921+58A>G	XP_006724730.1:n.6921+58A>G
XM_017029601.2:c.7110+58A>G	XP_016885090.1:n.7110+58A>G
XM_017029602.1:c.7080+58A>G	XP_016885091.1:n.7080+58A>G
XM_017029603.1:c.7032+58A>G	XP_016885092.1:n.7032+58A>G
XM_017029604.2:c.6999+58A>G	XP_016885093.1:n.6999+58A>G
XM_017029605.1:c.6996+58A>G	XP_016885094.1:n.6996+58A>G
XM_017029606.2:c.6969+58A>G	XP_016885095.1:n.6969+58A>G
XM_017029607.2:c.6966+58A>G	XP_016885096.1:n.6966+58A>G
XM_017029608.2:c.6918+58A>G	XP_016885097.1:n.6918+58A>G
XM_017029609.1:c.6882+58A>G	XP_016885098.1:n.6882+58A>G
XM_017029610.1:c.6879+58A>G	XP_016885099.1:n.6879+58A>G
XM_017029611.1:c.6834+58A>G	XP_016885100.1:n.6834+58A>G
XR_001755700.2:n.7499+58A>G
NM_138270.4:c.7086+58A>G	NP_612114.2:n.7086+58A>G
NM_000489.6:c.7200+58A>G MANE Select	NP_000480.3:n.7200+58A>G
NM_138270.5:c.7086+58A>G	NP_612114.2:n.7086+58A>G