Canonical Allele Identifier: CA2438929034

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508428G= , CM000685.2:g.77508428G=	GRCh38
NC_000023.10:g.76763906G= , CM000685.1:g.76763906G=	GRCh37
NC_000023.9:g.76650562G=	NCBI36
NG_008838.2:g.282794C=
NG_008838.3:g.282842C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7402C= MANE Select	ENSP00000362441.4:p.Gln2468=
ENST00000675732.1:c.2500C=	ENSP00000502598.1:p.Gln834=
ENST00000373344.9:c.7402C=	ENSP00000362441.4:p.Gln2468=
ENST00000395603.7:c.7288C=	ENSP00000378967.3:p.Gln2430=
ENST00000480283.5:c.*7030C=	ENSP00000480196.1:n.*7030C=
ENST00000623706.3:n.5722C=
NM_000489.4:c.7402C=	NP_000480.3:p.Gln2468=
NM_138270.3:c.7288C=	NP_612114.2:p.Gln2430=
XM_005262153.3:c.7399C=	XP_005262210.2:p.Gln2467=
XM_005262154.3:c.7315C=	XP_005262211.2:p.Gln2439=
XM_005262155.3:c.7285C=	XP_005262212.2:p.Gln2429=
XM_005262156.3:c.7237C=	XP_005262213.2:p.Gln2413=
XM_005262157.3:c.7198C=	XP_005262214.2:p.Gln2400=
XM_006724666.2:c.7285C=	XP_006724729.1:p.Gln2429=
XM_006724667.2:c.7123C=	XP_006724730.1:p.Gln2375=
XR_938400.1:n.8994C=
NM_000489.5:c.7402C=	NP_000480.3:p.Gln2468=
XM_005262153.5:c.7399C=	XP_005262210.2:p.Gln2467=
XM_005262154.5:c.7315C=	XP_005262211.2:p.Gln2439=
XM_005262155.4:c.7285C=	XP_005262212.2:p.Gln2429=
XM_005262156.4:c.7237C=	XP_005262213.2:p.Gln2413=
XM_005262157.5:c.7198C=	XP_005262214.2:p.Gln2400=
XM_006724666.4:c.7285C=	XP_006724729.1:p.Gln2429=
XM_006724667.3:c.7123C=	XP_006724730.1:p.Gln2375=
XM_017029601.2:c.7312C=	XP_016885090.1:p.Gln2438=
XM_017029602.1:c.7282C=	XP_016885091.1:p.Gln2428=
XM_017029603.1:c.7234C=	XP_016885092.1:p.Gln2412=
XM_017029604.2:c.7201C=	XP_016885093.1:p.Gln2401=
XM_017029605.1:c.7198C=	XP_016885094.1:p.Gln2400=
XM_017029606.2:c.7171C=	XP_016885095.1:p.Gln2391=
XM_017029607.2:c.7168C=	XP_016885096.1:p.Gln2390=
XM_017029608.2:c.7120C=	XP_016885097.1:p.Gln2374=
XM_017029609.1:c.7084C=	XP_016885098.1:p.Gln2362=
XM_017029610.1:c.7081C=	XP_016885099.1:p.Gln2361=
XM_017029611.1:c.7036C=	XP_016885100.1:p.Gln2346=
XR_001755700.2:n.7701C=
NM_138270.4:c.7288C=	NP_612114.2:p.Gln2430=
NM_000489.6:c.7402C= MANE Select	NP_000480.3:p.Gln2468=
NM_138270.5:c.7288C=	NP_612114.2:p.Gln2430=