Canonical Allele Identifier: CA413708639

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76907778C>A (hg19) ; chrX:g.77652288C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77652288C>A , CM000685.2:g.77652288C>A	GRCh38
NC_000023.10:g.76907778C>A , CM000685.1:g.76907778C>A	GRCh37
NC_000023.9:g.76794434C>A	NCBI36
NG_008838.2:g.138934G>T
NG_008838.3:g.138982G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4383G>T MANE Select	ENSP00000362441.4:p.Glu1461Asp
ENST00000373344.9:c.4383G>T	ENSP00000362441.4:p.Glu1461Asp
ENST00000395603.7:c.4269G>T	ENSP00000378967.3:p.Glu1423Asp
ENST00000480283.5:c.*4011G>T	ENSP00000480196.1:n.*4011G>T
NM_000489.4:c.4383G>T	NP_000480.3:p.Glu1461Asp
NM_138270.3:c.4269G>T	NP_612114.2:p.Glu1423Asp
XM_005262153.3:c.4380G>T	XP_005262210.2:p.Glu1460Asp
XM_005262154.3:c.4296G>T	XP_005262211.2:p.Glu1432Asp
XM_005262155.3:c.4266G>T	XP_005262212.2:p.Glu1422Asp
XM_005262156.3:c.4218G>T	XP_005262213.2:p.Glu1406Asp
XM_005262157.3:c.4179G>T	XP_005262214.2:p.Glu1393Asp
XM_006724666.2:c.4266G>T	XP_006724729.1:p.Glu1422Asp
XM_006724667.2:c.4104G>T	XP_006724730.1:p.Glu1368Asp
XM_006724668.2:c.4383G>T	XP_006724731.1:p.Glu1461Asp
XR_938400.1:n.4651G>T
NM_000489.5:c.4383G>T	NP_000480.3:p.Glu1461Asp
XM_005262153.5:c.4380G>T	XP_005262210.2:p.Glu1460Asp
XM_005262154.5:c.4296G>T	XP_005262211.2:p.Glu1432Asp
XM_005262155.4:c.4266G>T	XP_005262212.2:p.Glu1422Asp
XM_005262156.4:c.4218G>T	XP_005262213.2:p.Glu1406Asp
XM_005262157.5:c.4179G>T	XP_005262214.2:p.Glu1393Asp
XM_006724666.4:c.4266G>T	XP_006724729.1:p.Glu1422Asp
XM_006724667.3:c.4104G>T	XP_006724730.1:p.Glu1368Asp
XM_006724668.3:c.4383G>T	XP_006724731.1:p.Glu1461Asp
XM_017029601.2:c.4293G>T	XP_016885090.1:p.Glu1431Asp
XM_017029602.1:c.4263G>T	XP_016885091.1:p.Glu1421Asp
XM_017029603.1:c.4215G>T	XP_016885092.1:p.Glu1405Asp
XM_017029604.2:c.4182G>T	XP_016885093.1:p.Glu1394Asp
XM_017029605.1:c.4179G>T	XP_016885094.1:p.Glu1393Asp
XM_017029606.2:c.4152G>T	XP_016885095.1:p.Glu1384Asp
XM_017029607.2:c.4149G>T	XP_016885096.1:p.Glu1383Asp
XM_017029608.2:c.4101G>T	XP_016885097.1:p.Glu1367Asp
XM_017029609.1:c.4065G>T	XP_016885098.1:p.Glu1355Asp
XM_017029610.1:c.4062G>T	XP_016885099.1:p.Glu1354Asp
XM_017029611.1:c.4017G>T	XP_016885100.1:p.Glu1339Asp
XR_001755700.2:n.4608G>T
NM_138270.4:c.4269G>T	NP_612114.2:p.Glu1423Asp
NM_000489.6:c.4383G>T MANE Select	NP_000480.3:p.Glu1461Asp
NM_138270.5:c.4269G>T	NP_612114.2:p.Glu1423Asp