Canonical Allele Identifier: CA2438951450

Gene: ATRX

Linked Data

• dbSNP Id: rs2065536464

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574465T>C , CM000685.2:g.77574465T>C	GRCh38
NC_000023.10:g.76829930T>C , CM000685.1:g.76829930T>C	GRCh37
NC_000023.9:g.76716586T>C	NCBI36
NG_008838.2:g.216757A>G
NG_008838.3:g.216805A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6218-107A>G MANE Select	ENSP00000362441.4:n.6218-107A>G
ENST00000636152.1:n.53-107A>G
ENST00000675732.1:c.1316-107A>G	ENSP00000502598.1:n.1316-107A>G
ENST00000373344.9:c.6218-107A>G	ENSP00000362441.4:n.6218-107A>G
ENST00000395603.7:c.6104-107A>G	ENSP00000378967.3:n.6104-107A>G
ENST00000480283.5:c.*5846-107A>G	ENSP00000480196.1:n.*5846-107A>G
ENST00000623316.1:c.702-107A>G
ENST00000623706.3:n.3288-107A>G
NM_000489.4:c.6218-107A>G	NP_000480.3:n.6218-107A>G
NM_138270.3:c.6104-107A>G	NP_612114.2:n.6104-107A>G
XM_005262153.3:c.6215-107A>G	XP_005262210.2:n.6215-107A>G
XM_005262154.3:c.6131-107A>G	XP_005262211.2:n.6131-107A>G
XM_005262155.3:c.6101-107A>G	XP_005262212.2:n.6101-107A>G
XM_005262156.3:c.6053-107A>G	XP_005262213.2:n.6053-107A>G
XM_005262157.3:c.6014-107A>G	XP_005262214.2:n.6014-107A>G
XM_006724666.2:c.6101-107A>G	XP_006724729.1:n.6101-107A>G
XM_006724667.2:c.5939-107A>G	XP_006724730.1:n.5939-107A>G
XR_938400.1:n.6560-107A>G
NM_000489.5:c.6218-107A>G	NP_000480.3:n.6218-107A>G
XM_005262153.5:c.6215-107A>G	XP_005262210.2:n.6215-107A>G
XM_005262154.5:c.6131-107A>G	XP_005262211.2:n.6131-107A>G
XM_005262155.4:c.6101-107A>G	XP_005262212.2:n.6101-107A>G
XM_005262156.4:c.6053-107A>G	XP_005262213.2:n.6053-107A>G
XM_005262157.5:c.6014-107A>G	XP_005262214.2:n.6014-107A>G
XM_006724666.4:c.6101-107A>G	XP_006724729.1:n.6101-107A>G
XM_006724667.3:c.5939-107A>G	XP_006724730.1:n.5939-107A>G
XM_017029601.2:c.6128-107A>G	XP_016885090.1:n.6128-107A>G
XM_017029602.1:c.6098-107A>G	XP_016885091.1:n.6098-107A>G
XM_017029603.1:c.6050-107A>G	XP_016885092.1:n.6050-107A>G
XM_017029604.2:c.6017-107A>G	XP_016885093.1:n.6017-107A>G
XM_017029605.1:c.6014-107A>G	XP_016885094.1:n.6014-107A>G
XM_017029606.2:c.5987-107A>G	XP_016885095.1:n.5987-107A>G
XM_017029607.2:c.5984-107A>G	XP_016885096.1:n.5984-107A>G
XM_017029608.2:c.5936-107A>G	XP_016885097.1:n.5936-107A>G
XM_017029609.1:c.5900-107A>G	XP_016885098.1:n.5900-107A>G
XM_017029610.1:c.5897-107A>G	XP_016885099.1:n.5897-107A>G
XM_017029611.1:c.5852-107A>G	XP_016885100.1:n.5852-107A>G
XR_001755700.2:n.6517-107A>G
NM_138270.4:c.6104-107A>G	NP_612114.2:n.6104-107A>G
NM_000489.6:c.6218-107A>G MANE Select	NP_000480.3:n.6218-107A>G
NM_138270.5:c.6104-107A>G	NP_612114.2:n.6104-107A>G