Canonical Allele Identifier: CA413708941

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907824T>G (hg19) ; chrX:g.77652334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652334T>G , CM000685.2:g.77652334T>G	GRCh38
NC_000023.10:g.76907824T>G , CM000685.1:g.76907824T>G	GRCh37
NC_000023.9:g.76794480T>G	NCBI36
NG_008838.2:g.138888A>C
NG_008838.3:g.138936A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4337A>C MANE Select	ENSP00000362441.4:p.Glu1446Ala
ENST00000373344.9:c.4337A>C	ENSP00000362441.4:p.Glu1446Ala
ENST00000395603.7:c.4223A>C	ENSP00000378967.3:p.Glu1408Ala
ENST00000480283.5:c.*3965A>C	ENSP00000480196.1:n.*3965A>C
NM_000489.4:c.4337A>C	NP_000480.3:p.Glu1446Ala
NM_138270.3:c.4223A>C	NP_612114.2:p.Glu1408Ala
XM_005262153.3:c.4334A>C	XP_005262210.2:p.Glu1445Ala
XM_005262154.3:c.4250A>C	XP_005262211.2:p.Glu1417Ala
XM_005262155.3:c.4220A>C	XP_005262212.2:p.Glu1407Ala
XM_005262156.3:c.4172A>C	XP_005262213.2:p.Glu1391Ala
XM_005262157.3:c.4133A>C	XP_005262214.2:p.Glu1378Ala
XM_006724666.2:c.4220A>C	XP_006724729.1:p.Glu1407Ala
XM_006724667.2:c.4058A>C	XP_006724730.1:p.Glu1353Ala
XM_006724668.2:c.4337A>C	XP_006724731.1:p.Glu1446Ala
XR_938400.1:n.4605A>C
NM_000489.5:c.4337A>C	NP_000480.3:p.Glu1446Ala
XM_005262153.5:c.4334A>C	XP_005262210.2:p.Glu1445Ala
XM_005262154.5:c.4250A>C	XP_005262211.2:p.Glu1417Ala
XM_005262155.4:c.4220A>C	XP_005262212.2:p.Glu1407Ala
XM_005262156.4:c.4172A>C	XP_005262213.2:p.Glu1391Ala
XM_005262157.5:c.4133A>C	XP_005262214.2:p.Glu1378Ala
XM_006724666.4:c.4220A>C	XP_006724729.1:p.Glu1407Ala
XM_006724667.3:c.4058A>C	XP_006724730.1:p.Glu1353Ala
XM_006724668.3:c.4337A>C	XP_006724731.1:p.Glu1446Ala
XM_017029601.2:c.4247A>C	XP_016885090.1:p.Glu1416Ala
XM_017029602.1:c.4217A>C	XP_016885091.1:p.Glu1406Ala
XM_017029603.1:c.4169A>C	XP_016885092.1:p.Glu1390Ala
XM_017029604.2:c.4136A>C	XP_016885093.1:p.Glu1379Ala
XM_017029605.1:c.4133A>C	XP_016885094.1:p.Glu1378Ala
XM_017029606.2:c.4106A>C	XP_016885095.1:p.Glu1369Ala
XM_017029607.2:c.4103A>C	XP_016885096.1:p.Glu1368Ala
XM_017029608.2:c.4055A>C	XP_016885097.1:p.Glu1352Ala
XM_017029609.1:c.4019A>C	XP_016885098.1:p.Glu1340Ala
XM_017029610.1:c.4016A>C	XP_016885099.1:p.Glu1339Ala
XM_017029611.1:c.3971A>C	XP_016885100.1:p.Glu1324Ala
XR_001755700.2:n.4562A>C
NM_138270.4:c.4223A>C	NP_612114.2:p.Glu1408Ala
NM_000489.6:c.4337A>C MANE Select	NP_000480.3:p.Glu1446Ala
NM_138270.5:c.4223A>C	NP_612114.2:p.Glu1408Ala