Canonical Allele Identifier: CA2438929060
Gene: ATRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.77508519C= , CM000685.2:g.77508519C= GRCh38
NC_000023.10:g.76763997C= , CM000685.1:g.76763997C= GRCh37
NC_000023.9:g.76650653C= NCBI36
NG_008838.2:g.282703G=
NG_008838.3:g.282751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373344.11:c.7311G= MANE Select ENSP00000362441.4:p.Met2437=
ENST00000675732.1:c.2409G= ENSP00000502598.1:p.Met803=
ENST00000373344.9:c.7311G= ENSP00000362441.4:p.Met2437=
ENST00000395603.7:c.7197G= ENSP00000378967.3:p.Met2399=
ENST00000480283.5:c.*6939G= ENSP00000480196.1:n.*6939G=
ENST00000623706.3:n.5631G=
ENST00000624766.1:n.542G=
NM_000489.4:c.7311G= NP_000480.3:p.Met2437=
NM_138270.3:c.7197G= NP_612114.2:p.Met2399=
XM_005262153.3:c.7308G= XP_005262210.2:p.Met2436=
XM_005262154.3:c.7224G= XP_005262211.2:p.Met2408=
XM_005262155.3:c.7194G= XP_005262212.2:p.Met2398=
XM_005262156.3:c.7146G= XP_005262213.2:p.Met2382=
XM_005262157.3:c.7107G= XP_005262214.2:p.Met2369=
XM_006724666.2:c.7194G= XP_006724729.1:p.Met2398=
XM_006724667.2:c.7032G= XP_006724730.1:p.Met2344=
XR_938400.1:n.8903G=
NM_000489.5:c.7311G= NP_000480.3:p.Met2437=
XM_005262153.5:c.7308G= XP_005262210.2:p.Met2436=
XM_005262154.5:c.7224G= XP_005262211.2:p.Met2408=
XM_005262155.4:c.7194G= XP_005262212.2:p.Met2398=
XM_005262156.4:c.7146G= XP_005262213.2:p.Met2382=
XM_005262157.5:c.7107G= XP_005262214.2:p.Met2369=
XM_006724666.4:c.7194G= XP_006724729.1:p.Met2398=
XM_006724667.3:c.7032G= XP_006724730.1:p.Met2344=
XM_017029601.2:c.7221G= XP_016885090.1:p.Met2407=
XM_017029602.1:c.7191G= XP_016885091.1:p.Met2397=
XM_017029603.1:c.7143G= XP_016885092.1:p.Met2381=
XM_017029604.2:c.7110G= XP_016885093.1:p.Met2370=
XM_017029605.1:c.7107G= XP_016885094.1:p.Met2369=
XM_017029606.2:c.7080G= XP_016885095.1:p.Met2360=
XM_017029607.2:c.7077G= XP_016885096.1:p.Met2359=
XM_017029608.2:c.7029G= XP_016885097.1:p.Met2343=
XM_017029609.1:c.6993G= XP_016885098.1:p.Met2331=
XM_017029610.1:c.6990G= XP_016885099.1:p.Met2330=
XM_017029611.1:c.6945G= XP_016885100.1:p.Met2315=
XR_001755700.2:n.7610G=
NM_138270.4:c.7197G= NP_612114.2:p.Met2399=
NM_000489.6:c.7311G= MANE Select NP_000480.3:p.Met2437=
NM_138270.5:c.7197G= NP_612114.2:p.Met2399=