Canonical Allele Identifier: CA413703749

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763888G>T (hg19) ; chrX:g.77508410G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508410G>T , CM000685.2:g.77508410G>T	GRCh38
NC_000023.10:g.76763888G>T , CM000685.1:g.76763888G>T	GRCh37
NC_000023.9:g.76650544G>T	NCBI36
NG_008838.2:g.282812C>A
NG_008838.3:g.282860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7420C>A MANE Select	ENSP00000362441.4:p.Arg2474Ser
ENST00000675732.1:c.2518C>A	ENSP00000502598.1:p.Arg840Ser
ENST00000373344.9:c.7420C>A	ENSP00000362441.4:p.Arg2474Ser
ENST00000395603.7:c.7306C>A	ENSP00000378967.3:p.Arg2436Ser
ENST00000480283.5:c.*7048C>A	ENSP00000480196.1:n.*7048C>A
ENST00000623706.3:n.5740C>A
NM_000489.4:c.7420C>A	NP_000480.3:p.Arg2474Ser
NM_138270.3:c.7306C>A	NP_612114.2:p.Arg2436Ser
XM_005262153.3:c.7417C>A	XP_005262210.2:p.Arg2473Ser
XM_005262154.3:c.7333C>A	XP_005262211.2:p.Arg2445Ser
XM_005262155.3:c.7303C>A	XP_005262212.2:p.Arg2435Ser
XM_005262156.3:c.7255C>A	XP_005262213.2:p.Arg2419Ser
XM_005262157.3:c.7216C>A	XP_005262214.2:p.Arg2406Ser
XM_006724666.2:c.7303C>A	XP_006724729.1:p.Arg2435Ser
XM_006724667.2:c.7141C>A	XP_006724730.1:p.Arg2381Ser
XR_938400.1:n.9012C>A
NM_000489.5:c.7420C>A	NP_000480.3:p.Arg2474Ser
XM_005262153.5:c.7417C>A	XP_005262210.2:p.Arg2473Ser
XM_005262154.5:c.7333C>A	XP_005262211.2:p.Arg2445Ser
XM_005262155.4:c.7303C>A	XP_005262212.2:p.Arg2435Ser
XM_005262156.4:c.7255C>A	XP_005262213.2:p.Arg2419Ser
XM_005262157.5:c.7216C>A	XP_005262214.2:p.Arg2406Ser
XM_006724666.4:c.7303C>A	XP_006724729.1:p.Arg2435Ser
XM_006724667.3:c.7141C>A	XP_006724730.1:p.Arg2381Ser
XM_017029601.2:c.7330C>A	XP_016885090.1:p.Arg2444Ser
XM_017029602.1:c.7300C>A	XP_016885091.1:p.Arg2434Ser
XM_017029603.1:c.7252C>A	XP_016885092.1:p.Arg2418Ser
XM_017029604.2:c.7219C>A	XP_016885093.1:p.Arg2407Ser
XM_017029605.1:c.7216C>A	XP_016885094.1:p.Arg2406Ser
XM_017029606.2:c.7189C>A	XP_016885095.1:p.Arg2397Ser
XM_017029607.2:c.7186C>A	XP_016885096.1:p.Arg2396Ser
XM_017029608.2:c.7138C>A	XP_016885097.1:p.Arg2380Ser
XM_017029609.1:c.7102C>A	XP_016885098.1:p.Arg2368Ser
XM_017029610.1:c.7099C>A	XP_016885099.1:p.Arg2367Ser
XM_017029611.1:c.7054C>A	XP_016885100.1:p.Arg2352Ser
XR_001755700.2:n.7719C>A
NM_138270.4:c.7306C>A	NP_612114.2:p.Arg2436Ser
NM_000489.6:c.7420C>A MANE Select	NP_000480.3:p.Arg2474Ser
NM_138270.5:c.7306C>A	NP_612114.2:p.Arg2436Ser