Canonical Allele Identifier: CA413704685

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76764017C>A (hg19) ; chrX:g.77508539C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508539C>A , CM000685.2:g.77508539C>A	GRCh38
NC_000023.10:g.76764017C>A , CM000685.1:g.76764017C>A	GRCh37
NC_000023.9:g.76650673C>A	NCBI36
NG_008838.2:g.282683G>T
NG_008838.3:g.282731G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7291G>T MANE Select	ENSP00000362441.4:p.Ala2431Ser
ENST00000675732.1:c.2389G>T	ENSP00000502598.1:p.Ala797Ser
ENST00000373344.9:c.7291G>T	ENSP00000362441.4:p.Ala2431Ser
ENST00000395603.7:c.7177G>T	ENSP00000378967.3:p.Ala2393Ser
ENST00000480283.5:c.*6919G>T	ENSP00000480196.1:n.*6919G>T
ENST00000623706.3:n.5611G>T
ENST00000624766.1:n.522G>T
NM_000489.4:c.7291G>T	NP_000480.3:p.Ala2431Ser
NM_138270.3:c.7177G>T	NP_612114.2:p.Ala2393Ser
XM_005262153.3:c.7288G>T	XP_005262210.2:p.Ala2430Ser
XM_005262154.3:c.7204G>T	XP_005262211.2:p.Ala2402Ser
XM_005262155.3:c.7174G>T	XP_005262212.2:p.Ala2392Ser
XM_005262156.3:c.7126G>T	XP_005262213.2:p.Ala2376Ser
XM_005262157.3:c.7087G>T	XP_005262214.2:p.Ala2363Ser
XM_006724666.2:c.7174G>T	XP_006724729.1:p.Ala2392Ser
XM_006724667.2:c.7012G>T	XP_006724730.1:p.Ala2338Ser
XR_938400.1:n.8883G>T
NM_000489.5:c.7291G>T	NP_000480.3:p.Ala2431Ser
XM_005262153.5:c.7288G>T	XP_005262210.2:p.Ala2430Ser
XM_005262154.5:c.7204G>T	XP_005262211.2:p.Ala2402Ser
XM_005262155.4:c.7174G>T	XP_005262212.2:p.Ala2392Ser
XM_005262156.4:c.7126G>T	XP_005262213.2:p.Ala2376Ser
XM_005262157.5:c.7087G>T	XP_005262214.2:p.Ala2363Ser
XM_006724666.4:c.7174G>T	XP_006724729.1:p.Ala2392Ser
XM_006724667.3:c.7012G>T	XP_006724730.1:p.Ala2338Ser
XM_017029601.2:c.7201G>T	XP_016885090.1:p.Ala2401Ser
XM_017029602.1:c.7171G>T	XP_016885091.1:p.Ala2391Ser
XM_017029603.1:c.7123G>T	XP_016885092.1:p.Ala2375Ser
XM_017029604.2:c.7090G>T	XP_016885093.1:p.Ala2364Ser
XM_017029605.1:c.7087G>T	XP_016885094.1:p.Ala2363Ser
XM_017029606.2:c.7060G>T	XP_016885095.1:p.Ala2354Ser
XM_017029607.2:c.7057G>T	XP_016885096.1:p.Ala2353Ser
XM_017029608.2:c.7009G>T	XP_016885097.1:p.Ala2337Ser
XM_017029609.1:c.6973G>T	XP_016885098.1:p.Ala2325Ser
XM_017029610.1:c.6970G>T	XP_016885099.1:p.Ala2324Ser
XM_017029611.1:c.6925G>T	XP_016885100.1:p.Ala2309Ser
XR_001755700.2:n.7590G>T
NM_138270.4:c.7177G>T	NP_612114.2:p.Ala2393Ser
NM_000489.6:c.7291G>T MANE Select	NP_000480.3:p.Ala2431Ser
NM_138270.5:c.7177G>T	NP_612114.2:p.Ala2393Ser