Canonical Allele Identifier: CA517472950

Gene: ATRX

Linked Data

• gnomAD v4: X-77684431-G-A
• MyVariant Identifiers: chrX:g.76939923G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77684431G>A , CM000685.2:g.77684431G>A	GRCh38
NC_000023.10:g.76939923G>A , CM000685.1:g.76939923G>A	GRCh37
NC_000023.9:g.76826579G>A	NCBI36
NG_008838.2:g.106791C>T
NG_008838.3:g.106839C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.825C>T MANE Select	ENSP00000362441.4:p.Asp275=
ENST00000373344.9:c.825C>T	ENSP00000362441.4:p.Asp275=
ENST00000395603.7:c.711C>T	ENSP00000378967.3:p.Asp237=
ENST00000480283.5:c.*453C>T	ENSP00000480196.1:n.*453C>T
ENST00000623321.3:c.660C>T	ENSP00000485127.1:p.Asp220=
ENST00000624032.3:c.825C>T	ENSP00000485253.1:p.Asp275=
ENST00000624166.3:c.708C>T	ENSP00000485103.1:p.Asp236=
NM_000489.4:c.825C>T	NP_000480.3:p.Asp275=
NM_138270.3:c.711C>T	NP_612114.2:p.Asp237=
XM_005262153.3:c.822C>T	XP_005262210.2:p.Asp274=
XM_005262154.3:c.825C>T	XP_005262211.2:p.Asp275=
XM_005262155.3:c.708C>T	XP_005262212.2:p.Asp236=
XM_005262156.3:c.660C>T	XP_005262213.2:p.Asp220=
XM_005262157.3:c.708C>T	XP_005262214.2:p.Asp236=
XM_006724666.2:c.708C>T	XP_006724729.1:p.Asp236=
XM_006724667.2:c.546C>T	XP_006724730.1:p.Asp182=
XM_006724668.2:c.825C>T	XP_006724731.1:p.Asp275=
XR_938400.1:n.1093C>T
NM_000489.5:c.825C>T	NP_000480.3:p.Asp275=
XM_005262153.5:c.822C>T	XP_005262210.2:p.Asp274=
XM_005262154.5:c.825C>T	XP_005262211.2:p.Asp275=
XM_005262155.4:c.708C>T	XP_005262212.2:p.Asp236=
XM_005262156.4:c.660C>T	XP_005262213.2:p.Asp220=
XM_005262157.5:c.708C>T	XP_005262214.2:p.Asp236=
XM_006724666.4:c.708C>T	XP_006724729.1:p.Asp236=
XM_006724667.3:c.546C>T	XP_006724730.1:p.Asp182=
XM_006724668.3:c.825C>T	XP_006724731.1:p.Asp275=
XM_017029601.2:c.822C>T	XP_016885090.1:p.Asp274=
XM_017029602.1:c.705C>T	XP_016885091.1:p.Asp235=
XM_017029603.1:c.657C>T	XP_016885092.1:p.Asp219=
XM_017029604.2:c.711C>T	XP_016885093.1:p.Asp237=
XM_017029605.1:c.708C>T	XP_016885094.1:p.Asp236=
XM_017029606.2:c.594C>T	XP_016885095.1:p.Asp198=
XM_017029607.2:c.591C>T	XP_016885096.1:p.Asp197=
XM_017029608.2:c.543C>T	XP_016885097.1:p.Asp181=
XM_017029609.1:c.594C>T	XP_016885098.1:p.Asp198=
XM_017029610.1:c.591C>T	XP_016885099.1:p.Asp197=
XM_017029611.1:c.546C>T	XP_016885100.1:p.Asp182=
XR_001755700.2:n.1050C>T
NM_138270.4:c.711C>T	NP_612114.2:p.Asp237=
NM_000489.6:c.825C>T MANE Select	NP_000480.3:p.Asp275=
NM_138270.5:c.711C>T	NP_612114.2:p.Asp237=