Canonical Allele Identifier: CA413722496

Gene: ATRX

Linked Data

• ClinVar Variation Id: 1679127
• ClinVar RCV Id: RCV002226570
• dbSNP Id: rs2148656473
• gnomAD v4: X-77688847-G-A
• MyVariant Identifiers: chrX:g.76944340G>A (hg19) ; chrX:g.77688847G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77688847G>A , CM000685.2:g.77688847G>A	GRCh38
NC_000023.10:g.76944340G>A , CM000685.1:g.76944340G>A	GRCh37
NC_000023.9:g.76830996G>A	NCBI36
NG_008838.2:g.102375C>T
NG_008838.3:g.102423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.565C>T MANE Select	ENSP00000362441.4:p.His189Tyr
ENST00000373344.9:c.565C>T	ENSP00000362441.4:p.His189Tyr
ENST00000395603.7:c.451C>T	ENSP00000378967.3:p.His151Tyr
ENST00000480283.5:c.*193C>T	ENSP00000480196.1:n.*193C>T
ENST00000623321.3:c.400C>T	ENSP00000485127.1:p.His134Tyr
ENST00000624032.3:c.565C>T	ENSP00000485253.1:p.His189Tyr
ENST00000624166.3:c.448C>T	ENSP00000485103.1:p.His150Tyr
ENST00000624668.3:c.286C>T	ENSP00000485100.1:p.His96Tyr
ENST00000625063.3:c.380C>T
NM_000489.4:c.565C>T	NP_000480.3:p.His189Tyr
NM_138270.3:c.451C>T	NP_612114.2:p.His151Tyr
XM_005262153.3:c.562C>T	XP_005262210.2:p.His188Tyr
XM_005262154.3:c.565C>T	XP_005262211.2:p.His189Tyr
XM_005262155.3:c.448C>T	XP_005262212.2:p.His150Tyr
XM_005262156.3:c.400C>T	XP_005262213.2:p.His134Tyr
XM_005262157.3:c.448C>T	XP_005262214.2:p.His150Tyr
XM_006724666.2:c.448C>T	XP_006724729.1:p.His150Tyr
XM_006724667.2:c.286C>T	XP_006724730.1:p.His96Tyr
XM_006724668.2:c.565C>T	XP_006724731.1:p.His189Tyr
XR_938400.1:n.833C>T
NM_000489.5:c.565C>T	NP_000480.3:p.His189Tyr
XM_005262153.5:c.562C>T	XP_005262210.2:p.His188Tyr
XM_005262154.5:c.565C>T	XP_005262211.2:p.His189Tyr
XM_005262155.4:c.448C>T	XP_005262212.2:p.His150Tyr
XM_005262156.4:c.400C>T	XP_005262213.2:p.His134Tyr
XM_005262157.5:c.448C>T	XP_005262214.2:p.His150Tyr
XM_006724666.4:c.448C>T	XP_006724729.1:p.His150Tyr
XM_006724667.3:c.286C>T	XP_006724730.1:p.His96Tyr
XM_006724668.3:c.565C>T	XP_006724731.1:p.His189Tyr
XM_017029601.2:c.562C>T	XP_016885090.1:p.His188Tyr
XM_017029602.1:c.445C>T	XP_016885091.1:p.His149Tyr
XM_017029603.1:c.397C>T	XP_016885092.1:p.His133Tyr
XM_017029604.2:c.451C>T	XP_016885093.1:p.His151Tyr
XM_017029605.1:c.448C>T	XP_016885094.1:p.His150Tyr
XM_017029606.2:c.334C>T	XP_016885095.1:p.His112Tyr
XM_017029607.2:c.331C>T	XP_016885096.1:p.His111Tyr
XM_017029608.2:c.283C>T	XP_016885097.1:p.His95Tyr
XM_017029609.1:c.334C>T	XP_016885098.1:p.His112Tyr
XM_017029610.1:c.331C>T	XP_016885099.1:p.His111Tyr
XM_017029611.1:c.286C>T	XP_016885100.1:p.His96Tyr
XR_001755700.2:n.790C>T
NM_138270.4:c.451C>T	NP_612114.2:p.His151Tyr
NM_000489.6:c.565C>T MANE Select	NP_000480.3:p.His189Tyr
NM_138270.5:c.451C>T	NP_612114.2:p.His151Tyr