Canonical Allele Identifier: CA2738745702

Gene: ATRX

Linked Data

• dbSNP Id: rs2148441283

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652386A>C , CM000685.2:g.77652386A>C	GRCh38
NC_000023.10:g.76907876A>C , CM000685.1:g.76907876A>C	GRCh37
NC_000023.9:g.76794532A>C	NCBI36
NG_008838.2:g.138836T>G
NG_008838.3:g.138884T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4318-33T>G MANE Select	ENSP00000362441.4:n.4318-33T>G
ENST00000373344.9:c.4318-33T>G	ENSP00000362441.4:n.4318-33T>G
ENST00000395603.7:c.4204-33T>G	ENSP00000378967.3:n.4204-33T>G
ENST00000480283.5:c.*3946-33T>G	ENSP00000480196.1:n.*3946-33T>G
NM_000489.4:c.4318-33T>G	NP_000480.3:n.4318-33T>G
NM_138270.3:c.4204-33T>G	NP_612114.2:n.4204-33T>G
XM_005262153.3:c.4315-33T>G	XP_005262210.2:n.4315-33T>G
XM_005262154.3:c.4231-33T>G	XP_005262211.2:n.4231-33T>G
XM_005262155.3:c.4201-33T>G	XP_005262212.2:n.4201-33T>G
XM_005262156.3:c.4153-33T>G	XP_005262213.2:n.4153-33T>G
XM_005262157.3:c.4114-33T>G	XP_005262214.2:n.4114-33T>G
XM_006724666.2:c.4201-33T>G	XP_006724729.1:n.4201-33T>G
XM_006724667.2:c.4039-33T>G	XP_006724730.1:n.4039-33T>G
XM_006724668.2:c.4318-33T>G	XP_006724731.1:n.4318-33T>G
XR_938400.1:n.4586-33T>G
NM_000489.5:c.4318-33T>G	NP_000480.3:n.4318-33T>G
XM_005262153.5:c.4315-33T>G	XP_005262210.2:n.4315-33T>G
XM_005262154.5:c.4231-33T>G	XP_005262211.2:n.4231-33T>G
XM_005262155.4:c.4201-33T>G	XP_005262212.2:n.4201-33T>G
XM_005262156.4:c.4153-33T>G	XP_005262213.2:n.4153-33T>G
XM_005262157.5:c.4114-33T>G	XP_005262214.2:n.4114-33T>G
XM_006724666.4:c.4201-33T>G	XP_006724729.1:n.4201-33T>G
XM_006724667.3:c.4039-33T>G	XP_006724730.1:n.4039-33T>G
XM_006724668.3:c.4318-33T>G	XP_006724731.1:n.4318-33T>G
XM_017029601.2:c.4228-33T>G	XP_016885090.1:n.4228-33T>G
XM_017029602.1:c.4198-33T>G	XP_016885091.1:n.4198-33T>G
XM_017029603.1:c.4150-33T>G	XP_016885092.1:n.4150-33T>G
XM_017029604.2:c.4117-33T>G	XP_016885093.1:n.4117-33T>G
XM_017029605.1:c.4114-33T>G	XP_016885094.1:n.4114-33T>G
XM_017029606.2:c.4087-33T>G	XP_016885095.1:n.4087-33T>G
XM_017029607.2:c.4084-33T>G	XP_016885096.1:n.4084-33T>G
XM_017029608.2:c.4036-33T>G	XP_016885097.1:n.4036-33T>G
XM_017029609.1:c.4000-33T>G	XP_016885098.1:n.4000-33T>G
XM_017029610.1:c.3997-33T>G	XP_016885099.1:n.3997-33T>G
XM_017029611.1:c.3952-33T>G	XP_016885100.1:n.3952-33T>G
XR_001755700.2:n.4543-33T>G
NM_138270.4:c.4204-33T>G	NP_612114.2:n.4204-33T>G
NM_000489.6:c.4318-33T>G MANE Select	NP_000480.3:n.4318-33T>G
NM_138270.5:c.4204-33T>G	NP_612114.2:n.4204-33T>G