Canonical Allele Identifier: CA413708248

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907713A>C (hg19) ; chrX:g.77652223A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652223A>C , CM000685.2:g.77652223A>C	GRCh38
NC_000023.10:g.76907713A>C , CM000685.1:g.76907713A>C	GRCh37
NC_000023.9:g.76794369A>C	NCBI36
NG_008838.2:g.138999T>G
NG_008838.3:g.139047T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4448T>G MANE Select	ENSP00000362441.4:p.Ile1483Ser
ENST00000373344.9:c.4448T>G	ENSP00000362441.4:p.Ile1483Ser
ENST00000395603.7:c.4334T>G	ENSP00000378967.3:p.Ile1445Ser
ENST00000480283.5:c.*4076T>G	ENSP00000480196.1:n.*4076T>G
ENST00000623242.3:c.54T>G
NM_000489.4:c.4448T>G	NP_000480.3:p.Ile1483Ser
NM_138270.3:c.4334T>G	NP_612114.2:p.Ile1445Ser
XM_005262153.3:c.4445T>G	XP_005262210.2:p.Ile1482Ser
XM_005262154.3:c.4361T>G	XP_005262211.2:p.Ile1454Ser
XM_005262155.3:c.4331T>G	XP_005262212.2:p.Ile1444Ser
XM_005262156.3:c.4283T>G	XP_005262213.2:p.Ile1428Ser
XM_005262157.3:c.4244T>G	XP_005262214.2:p.Ile1415Ser
XM_006724666.2:c.4331T>G	XP_006724729.1:p.Ile1444Ser
XM_006724667.2:c.4169T>G	XP_006724730.1:p.Ile1390Ser
XM_006724668.2:c.4448T>G	XP_006724731.1:p.Ile1483Ser
XR_938400.1:n.4716T>G
NM_000489.5:c.4448T>G	NP_000480.3:p.Ile1483Ser
XM_005262153.5:c.4445T>G	XP_005262210.2:p.Ile1482Ser
XM_005262154.5:c.4361T>G	XP_005262211.2:p.Ile1454Ser
XM_005262155.4:c.4331T>G	XP_005262212.2:p.Ile1444Ser
XM_005262156.4:c.4283T>G	XP_005262213.2:p.Ile1428Ser
XM_005262157.5:c.4244T>G	XP_005262214.2:p.Ile1415Ser
XM_006724666.4:c.4331T>G	XP_006724729.1:p.Ile1444Ser
XM_006724667.3:c.4169T>G	XP_006724730.1:p.Ile1390Ser
XM_006724668.3:c.4448T>G	XP_006724731.1:p.Ile1483Ser
XM_017029601.2:c.4358T>G	XP_016885090.1:p.Ile1453Ser
XM_017029602.1:c.4328T>G	XP_016885091.1:p.Ile1443Ser
XM_017029603.1:c.4280T>G	XP_016885092.1:p.Ile1427Ser
XM_017029604.2:c.4247T>G	XP_016885093.1:p.Ile1416Ser
XM_017029605.1:c.4244T>G	XP_016885094.1:p.Ile1415Ser
XM_017029606.2:c.4217T>G	XP_016885095.1:p.Ile1406Ser
XM_017029607.2:c.4214T>G	XP_016885096.1:p.Ile1405Ser
XM_017029608.2:c.4166T>G	XP_016885097.1:p.Ile1389Ser
XM_017029609.1:c.4130T>G	XP_016885098.1:p.Ile1377Ser
XM_017029610.1:c.4127T>G	XP_016885099.1:p.Ile1376Ser
XM_017029611.1:c.4082T>G	XP_016885100.1:p.Ile1361Ser
XR_001755700.2:n.4673T>G
NM_138270.4:c.4334T>G	NP_612114.2:p.Ile1445Ser
NM_000489.6:c.4448T>G MANE Select	NP_000480.3:p.Ile1483Ser
NM_138270.5:c.4334T>G	NP_612114.2:p.Ile1445Ser