Canonical Allele Identifier: CA413708308

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907725T>G (hg19) ; chrX:g.77652235T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652235T>G , CM000685.2:g.77652235T>G	GRCh38
NC_000023.10:g.76907725T>G , CM000685.1:g.76907725T>G	GRCh37
NC_000023.9:g.76794381T>G	NCBI36
NG_008838.2:g.138987A>C
NG_008838.3:g.139035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4436A>C MANE Select	ENSP00000362441.4:p.Lys1479Thr
ENST00000373344.9:c.4436A>C	ENSP00000362441.4:p.Lys1479Thr
ENST00000395603.7:c.4322A>C	ENSP00000378967.3:p.Lys1441Thr
ENST00000480283.5:c.*4064A>C	ENSP00000480196.1:n.*4064A>C
ENST00000623242.3:c.42A>C
NM_000489.4:c.4436A>C	NP_000480.3:p.Lys1479Thr
NM_138270.3:c.4322A>C	NP_612114.2:p.Lys1441Thr
XM_005262153.3:c.4433A>C	XP_005262210.2:p.Lys1478Thr
XM_005262154.3:c.4349A>C	XP_005262211.2:p.Lys1450Thr
XM_005262155.3:c.4319A>C	XP_005262212.2:p.Lys1440Thr
XM_005262156.3:c.4271A>C	XP_005262213.2:p.Lys1424Thr
XM_005262157.3:c.4232A>C	XP_005262214.2:p.Lys1411Thr
XM_006724666.2:c.4319A>C	XP_006724729.1:p.Lys1440Thr
XM_006724667.2:c.4157A>C	XP_006724730.1:p.Lys1386Thr
XM_006724668.2:c.4436A>C	XP_006724731.1:p.Lys1479Thr
XR_938400.1:n.4704A>C
NM_000489.5:c.4436A>C	NP_000480.3:p.Lys1479Thr
XM_005262153.5:c.4433A>C	XP_005262210.2:p.Lys1478Thr
XM_005262154.5:c.4349A>C	XP_005262211.2:p.Lys1450Thr
XM_005262155.4:c.4319A>C	XP_005262212.2:p.Lys1440Thr
XM_005262156.4:c.4271A>C	XP_005262213.2:p.Lys1424Thr
XM_005262157.5:c.4232A>C	XP_005262214.2:p.Lys1411Thr
XM_006724666.4:c.4319A>C	XP_006724729.1:p.Lys1440Thr
XM_006724667.3:c.4157A>C	XP_006724730.1:p.Lys1386Thr
XM_006724668.3:c.4436A>C	XP_006724731.1:p.Lys1479Thr
XM_017029601.2:c.4346A>C	XP_016885090.1:p.Lys1449Thr
XM_017029602.1:c.4316A>C	XP_016885091.1:p.Lys1439Thr
XM_017029603.1:c.4268A>C	XP_016885092.1:p.Lys1423Thr
XM_017029604.2:c.4235A>C	XP_016885093.1:p.Lys1412Thr
XM_017029605.1:c.4232A>C	XP_016885094.1:p.Lys1411Thr
XM_017029606.2:c.4205A>C	XP_016885095.1:p.Lys1402Thr
XM_017029607.2:c.4202A>C	XP_016885096.1:p.Lys1401Thr
XM_017029608.2:c.4154A>C	XP_016885097.1:p.Lys1385Thr
XM_017029609.1:c.4118A>C	XP_016885098.1:p.Lys1373Thr
XM_017029610.1:c.4115A>C	XP_016885099.1:p.Lys1372Thr
XM_017029611.1:c.4070A>C	XP_016885100.1:p.Lys1357Thr
XR_001755700.2:n.4661A>C
NM_138270.4:c.4322A>C	NP_612114.2:p.Lys1441Thr
NM_000489.6:c.4436A>C MANE Select	NP_000480.3:p.Lys1479Thr
NM_138270.5:c.4322A>C	NP_612114.2:p.Lys1441Thr