Canonical Allele Identifier: CA413703978

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763921C>T (hg19) ; chrX:g.77508443C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508443C>T , CM000685.2:g.77508443C>T	GRCh38
NC_000023.10:g.76763921C>T , CM000685.1:g.76763921C>T	GRCh37
NC_000023.9:g.76650577C>T	NCBI36
NG_008838.2:g.282779G>A
NG_008838.3:g.282827G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7387G>A MANE Select	ENSP00000362441.4:p.Val2463Met
ENST00000675732.1:c.2485G>A	ENSP00000502598.1:p.Val829Met
ENST00000373344.9:c.7387G>A	ENSP00000362441.4:p.Val2463Met
ENST00000395603.7:c.7273G>A	ENSP00000378967.3:p.Val2425Met
ENST00000480283.5:c.*7015G>A	ENSP00000480196.1:n.*7015G>A
ENST00000623706.3:n.5707G>A
NM_000489.4:c.7387G>A	NP_000480.3:p.Val2463Met
NM_138270.3:c.7273G>A	NP_612114.2:p.Val2425Met
XM_005262153.3:c.7384G>A	XP_005262210.2:p.Val2462Met
XM_005262154.3:c.7300G>A	XP_005262211.2:p.Val2434Met
XM_005262155.3:c.7270G>A	XP_005262212.2:p.Val2424Met
XM_005262156.3:c.7222G>A	XP_005262213.2:p.Val2408Met
XM_005262157.3:c.7183G>A	XP_005262214.2:p.Val2395Met
XM_006724666.2:c.7270G>A	XP_006724729.1:p.Val2424Met
XM_006724667.2:c.7108G>A	XP_006724730.1:p.Val2370Met
XR_938400.1:n.8979G>A
NM_000489.5:c.7387G>A	NP_000480.3:p.Val2463Met
XM_005262153.5:c.7384G>A	XP_005262210.2:p.Val2462Met
XM_005262154.5:c.7300G>A	XP_005262211.2:p.Val2434Met
XM_005262155.4:c.7270G>A	XP_005262212.2:p.Val2424Met
XM_005262156.4:c.7222G>A	XP_005262213.2:p.Val2408Met
XM_005262157.5:c.7183G>A	XP_005262214.2:p.Val2395Met
XM_006724666.4:c.7270G>A	XP_006724729.1:p.Val2424Met
XM_006724667.3:c.7108G>A	XP_006724730.1:p.Val2370Met
XM_017029601.2:c.7297G>A	XP_016885090.1:p.Val2433Met
XM_017029602.1:c.7267G>A	XP_016885091.1:p.Val2423Met
XM_017029603.1:c.7219G>A	XP_016885092.1:p.Val2407Met
XM_017029604.2:c.7186G>A	XP_016885093.1:p.Val2396Met
XM_017029605.1:c.7183G>A	XP_016885094.1:p.Val2395Met
XM_017029606.2:c.7156G>A	XP_016885095.1:p.Val2386Met
XM_017029607.2:c.7153G>A	XP_016885096.1:p.Val2385Met
XM_017029608.2:c.7105G>A	XP_016885097.1:p.Val2369Met
XM_017029609.1:c.7069G>A	XP_016885098.1:p.Val2357Met
XM_017029610.1:c.7066G>A	XP_016885099.1:p.Val2356Met
XM_017029611.1:c.7021G>A	XP_016885100.1:p.Val2341Met
XR_001755700.2:n.7686G>A
NM_138270.4:c.7273G>A	NP_612114.2:p.Val2425Met
NM_000489.6:c.7387G>A MANE Select	NP_000480.3:p.Val2463Met
NM_138270.5:c.7273G>A	NP_612114.2:p.Val2425Met