Canonical Allele Identifier: CA413704705

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764019T>G (hg19) ; chrX:g.77508541T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508541T>G , CM000685.2:g.77508541T>G	GRCh38
NC_000023.10:g.76764019T>G , CM000685.1:g.76764019T>G	GRCh37
NC_000023.9:g.76650675T>G	NCBI36
NG_008838.2:g.282681A>C
NG_008838.3:g.282729A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7289A>C MANE Select	ENSP00000362441.4:p.Gln2430Pro
ENST00000675732.1:c.2387A>C	ENSP00000502598.1:p.Gln796Pro
ENST00000373344.9:c.7289A>C	ENSP00000362441.4:p.Gln2430Pro
ENST00000395603.7:c.7175A>C	ENSP00000378967.3:p.Gln2392Pro
ENST00000480283.5:c.*6917A>C	ENSP00000480196.1:n.*6917A>C
ENST00000623706.3:n.5609A>C
ENST00000624766.1:n.520A>C
NM_000489.4:c.7289A>C	NP_000480.3:p.Gln2430Pro
NM_138270.3:c.7175A>C	NP_612114.2:p.Gln2392Pro
XM_005262153.3:c.7286A>C	XP_005262210.2:p.Gln2429Pro
XM_005262154.3:c.7202A>C	XP_005262211.2:p.Gln2401Pro
XM_005262155.3:c.7172A>C	XP_005262212.2:p.Gln2391Pro
XM_005262156.3:c.7124A>C	XP_005262213.2:p.Gln2375Pro
XM_005262157.3:c.7085A>C	XP_005262214.2:p.Gln2362Pro
XM_006724666.2:c.7172A>C	XP_006724729.1:p.Gln2391Pro
XM_006724667.2:c.7010A>C	XP_006724730.1:p.Gln2337Pro
XR_938400.1:n.8881A>C
NM_000489.5:c.7289A>C	NP_000480.3:p.Gln2430Pro
XM_005262153.5:c.7286A>C	XP_005262210.2:p.Gln2429Pro
XM_005262154.5:c.7202A>C	XP_005262211.2:p.Gln2401Pro
XM_005262155.4:c.7172A>C	XP_005262212.2:p.Gln2391Pro
XM_005262156.4:c.7124A>C	XP_005262213.2:p.Gln2375Pro
XM_005262157.5:c.7085A>C	XP_005262214.2:p.Gln2362Pro
XM_006724666.4:c.7172A>C	XP_006724729.1:p.Gln2391Pro
XM_006724667.3:c.7010A>C	XP_006724730.1:p.Gln2337Pro
XM_017029601.2:c.7199A>C	XP_016885090.1:p.Gln2400Pro
XM_017029602.1:c.7169A>C	XP_016885091.1:p.Gln2390Pro
XM_017029603.1:c.7121A>C	XP_016885092.1:p.Gln2374Pro
XM_017029604.2:c.7088A>C	XP_016885093.1:p.Gln2363Pro
XM_017029605.1:c.7085A>C	XP_016885094.1:p.Gln2362Pro
XM_017029606.2:c.7058A>C	XP_016885095.1:p.Gln2353Pro
XM_017029607.2:c.7055A>C	XP_016885096.1:p.Gln2352Pro
XM_017029608.2:c.7007A>C	XP_016885097.1:p.Gln2336Pro
XM_017029609.1:c.6971A>C	XP_016885098.1:p.Gln2324Pro
XM_017029610.1:c.6968A>C	XP_016885099.1:p.Gln2323Pro
XM_017029611.1:c.6923A>C	XP_016885100.1:p.Gln2308Pro
XR_001755700.2:n.7588A>C
NM_138270.4:c.7175A>C	NP_612114.2:p.Gln2392Pro
NM_000489.6:c.7289A>C MANE Select	NP_000480.3:p.Gln2430Pro
NM_138270.5:c.7175A>C	NP_612114.2:p.Gln2392Pro