Canonical Allele Identifier: CA413703787

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763893A>C (hg19) ; chrX:g.77508415A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508415A>C , CM000685.2:g.77508415A>C	GRCh38
NC_000023.10:g.76763893A>C , CM000685.1:g.76763893A>C	GRCh37
NC_000023.9:g.76650549A>C	NCBI36
NG_008838.2:g.282807T>G
NG_008838.3:g.282855T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7415T>G MANE Select	ENSP00000362441.4:p.Leu2472Ter
ENST00000675732.1:c.2513T>G	ENSP00000502598.1:p.Leu838Ter
ENST00000373344.9:c.7415T>G	ENSP00000362441.4:p.Leu2472Ter
ENST00000395603.7:c.7301T>G	ENSP00000378967.3:p.Leu2434Ter
ENST00000480283.5:c.*7043T>G	ENSP00000480196.1:n.*7043T>G
ENST00000623706.3:n.5735T>G
NM_000489.4:c.7415T>G	NP_000480.3:p.Leu2472Ter
NM_138270.3:c.7301T>G	NP_612114.2:p.Leu2434Ter
XM_005262153.3:c.7412T>G	XP_005262210.2:p.Leu2471Ter
XM_005262154.3:c.7328T>G	XP_005262211.2:p.Leu2443Ter
XM_005262155.3:c.7298T>G	XP_005262212.2:p.Leu2433Ter
XM_005262156.3:c.7250T>G	XP_005262213.2:p.Leu2417Ter
XM_005262157.3:c.7211T>G	XP_005262214.2:p.Leu2404Ter
XM_006724666.2:c.7298T>G	XP_006724729.1:p.Leu2433Ter
XM_006724667.2:c.7136T>G	XP_006724730.1:p.Leu2379Ter
XR_938400.1:n.9007T>G
NM_000489.5:c.7415T>G	NP_000480.3:p.Leu2472Ter
XM_005262153.5:c.7412T>G	XP_005262210.2:p.Leu2471Ter
XM_005262154.5:c.7328T>G	XP_005262211.2:p.Leu2443Ter
XM_005262155.4:c.7298T>G	XP_005262212.2:p.Leu2433Ter
XM_005262156.4:c.7250T>G	XP_005262213.2:p.Leu2417Ter
XM_005262157.5:c.7211T>G	XP_005262214.2:p.Leu2404Ter
XM_006724666.4:c.7298T>G	XP_006724729.1:p.Leu2433Ter
XM_006724667.3:c.7136T>G	XP_006724730.1:p.Leu2379Ter
XM_017029601.2:c.7325T>G	XP_016885090.1:p.Leu2442Ter
XM_017029602.1:c.7295T>G	XP_016885091.1:p.Leu2432Ter
XM_017029603.1:c.7247T>G	XP_016885092.1:p.Leu2416Ter
XM_017029604.2:c.7214T>G	XP_016885093.1:p.Leu2405Ter
XM_017029605.1:c.7211T>G	XP_016885094.1:p.Leu2404Ter
XM_017029606.2:c.7184T>G	XP_016885095.1:p.Leu2395Ter
XM_017029607.2:c.7181T>G	XP_016885096.1:p.Leu2394Ter
XM_017029608.2:c.7133T>G	XP_016885097.1:p.Leu2378Ter
XM_017029609.1:c.7097T>G	XP_016885098.1:p.Leu2366Ter
XM_017029610.1:c.7094T>G	XP_016885099.1:p.Leu2365Ter
XM_017029611.1:c.7049T>G	XP_016885100.1:p.Leu2350Ter
XR_001755700.2:n.7714T>G
NM_138270.4:c.7301T>G	NP_612114.2:p.Leu2434Ter
NM_000489.6:c.7415T>G MANE Select	NP_000480.3:p.Leu2472Ter
NM_138270.5:c.7301T>G	NP_612114.2:p.Leu2434Ter