Canonical Allele Identifier: CA413704831

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764033T>G (hg19) ; chrX:g.77508555T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508555T>G , CM000685.2:g.77508555T>G	GRCh38
NC_000023.10:g.76764033T>G , CM000685.1:g.76764033T>G	GRCh37
NC_000023.9:g.76650689T>G	NCBI36
NG_008838.2:g.282667A>C
NG_008838.3:g.282715A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7275A>C MANE Select	ENSP00000362441.4:p.Gln2425His
ENST00000675732.1:c.2373A>C	ENSP00000502598.1:p.Gln791His
ENST00000373344.9:c.7275A>C	ENSP00000362441.4:p.Gln2425His
ENST00000395603.7:c.7161A>C	ENSP00000378967.3:p.Gln2387His
ENST00000480283.5:c.*6903A>C	ENSP00000480196.1:n.*6903A>C
ENST00000623706.3:n.5595A>C
ENST00000624766.1:n.506A>C
NM_000489.4:c.7275A>C	NP_000480.3:p.Gln2425His
NM_138270.3:c.7161A>C	NP_612114.2:p.Gln2387His
XM_005262153.3:c.7272A>C	XP_005262210.2:p.Gln2424His
XM_005262154.3:c.7188A>C	XP_005262211.2:p.Gln2396His
XM_005262155.3:c.7158A>C	XP_005262212.2:p.Gln2386His
XM_005262156.3:c.7110A>C	XP_005262213.2:p.Gln2370His
XM_005262157.3:c.7071A>C	XP_005262214.2:p.Gln2357His
XM_006724666.2:c.7158A>C	XP_006724729.1:p.Gln2386His
XM_006724667.2:c.6996A>C	XP_006724730.1:p.Gln2332His
XR_938400.1:n.8867A>C
NM_000489.5:c.7275A>C	NP_000480.3:p.Gln2425His
XM_005262153.5:c.7272A>C	XP_005262210.2:p.Gln2424His
XM_005262154.5:c.7188A>C	XP_005262211.2:p.Gln2396His
XM_005262155.4:c.7158A>C	XP_005262212.2:p.Gln2386His
XM_005262156.4:c.7110A>C	XP_005262213.2:p.Gln2370His
XM_005262157.5:c.7071A>C	XP_005262214.2:p.Gln2357His
XM_006724666.4:c.7158A>C	XP_006724729.1:p.Gln2386His
XM_006724667.3:c.6996A>C	XP_006724730.1:p.Gln2332His
XM_017029601.2:c.7185A>C	XP_016885090.1:p.Gln2395His
XM_017029602.1:c.7155A>C	XP_016885091.1:p.Gln2385His
XM_017029603.1:c.7107A>C	XP_016885092.1:p.Gln2369His
XM_017029604.2:c.7074A>C	XP_016885093.1:p.Gln2358His
XM_017029605.1:c.7071A>C	XP_016885094.1:p.Gln2357His
XM_017029606.2:c.7044A>C	XP_016885095.1:p.Gln2348His
XM_017029607.2:c.7041A>C	XP_016885096.1:p.Gln2347His
XM_017029608.2:c.6993A>C	XP_016885097.1:p.Gln2331His
XM_017029609.1:c.6957A>C	XP_016885098.1:p.Gln2319His
XM_017029610.1:c.6954A>C	XP_016885099.1:p.Gln2318His
XM_017029611.1:c.6909A>C	XP_016885100.1:p.Gln2303His
XR_001755700.2:n.7574A>C
NM_138270.4:c.7161A>C	NP_612114.2:p.Gln2387His
NM_000489.6:c.7275A>C MANE Select	NP_000480.3:p.Gln2425His
NM_138270.5:c.7161A>C	NP_612114.2:p.Gln2387His