Canonical Allele Identifier: CA2438929035

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508429C= , CM000685.2:g.77508429C=	GRCh38
NC_000023.10:g.76763907C= , CM000685.1:g.76763907C=	GRCh37
NC_000023.9:g.76650563C=	NCBI36
NG_008838.2:g.282793G=
NG_008838.3:g.282841G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7401G= MANE Select	ENSP00000362441.4:p.Met2467=
ENST00000675732.1:c.2499G=	ENSP00000502598.1:p.Met833=
ENST00000373344.9:c.7401G=	ENSP00000362441.4:p.Met2467=
ENST00000395603.7:c.7287G=	ENSP00000378967.3:p.Met2429=
ENST00000480283.5:c.*7029G=	ENSP00000480196.1:n.*7029G=
ENST00000623706.3:n.5721G=
NM_000489.4:c.7401G=	NP_000480.3:p.Met2467=
NM_138270.3:c.7287G=	NP_612114.2:p.Met2429=
XM_005262153.3:c.7398G=	XP_005262210.2:p.Met2466=
XM_005262154.3:c.7314G=	XP_005262211.2:p.Met2438=
XM_005262155.3:c.7284G=	XP_005262212.2:p.Met2428=
XM_005262156.3:c.7236G=	XP_005262213.2:p.Met2412=
XM_005262157.3:c.7197G=	XP_005262214.2:p.Met2399=
XM_006724666.2:c.7284G=	XP_006724729.1:p.Met2428=
XM_006724667.2:c.7122G=	XP_006724730.1:p.Met2374=
XR_938400.1:n.8993G=
NM_000489.5:c.7401G=	NP_000480.3:p.Met2467=
XM_005262153.5:c.7398G=	XP_005262210.2:p.Met2466=
XM_005262154.5:c.7314G=	XP_005262211.2:p.Met2438=
XM_005262155.4:c.7284G=	XP_005262212.2:p.Met2428=
XM_005262156.4:c.7236G=	XP_005262213.2:p.Met2412=
XM_005262157.5:c.7197G=	XP_005262214.2:p.Met2399=
XM_006724666.4:c.7284G=	XP_006724729.1:p.Met2428=
XM_006724667.3:c.7122G=	XP_006724730.1:p.Met2374=
XM_017029601.2:c.7311G=	XP_016885090.1:p.Met2437=
XM_017029602.1:c.7281G=	XP_016885091.1:p.Met2427=
XM_017029603.1:c.7233G=	XP_016885092.1:p.Met2411=
XM_017029604.2:c.7200G=	XP_016885093.1:p.Met2400=
XM_017029605.1:c.7197G=	XP_016885094.1:p.Met2399=
XM_017029606.2:c.7170G=	XP_016885095.1:p.Met2390=
XM_017029607.2:c.7167G=	XP_016885096.1:p.Met2389=
XM_017029608.2:c.7119G=	XP_016885097.1:p.Met2373=
XM_017029609.1:c.7083G=	XP_016885098.1:p.Met2361=
XM_017029610.1:c.7080G=	XP_016885099.1:p.Met2360=
XM_017029611.1:c.7035G=	XP_016885100.1:p.Met2345=
XR_001755700.2:n.7700G=
NM_138270.4:c.7287G=	NP_612114.2:p.Met2429=
NM_000489.6:c.7401G= MANE Select	NP_000480.3:p.Met2467=
NM_138270.5:c.7287G=	NP_612114.2:p.Met2429=