Canonical Allele Identifier: CA517374779

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829765T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574300T>C , CM000685.2:g.77574300T>C	GRCh38
NC_000023.10:g.76829765T>C , CM000685.1:g.76829765T>C	GRCh37
NC_000023.9:g.76716421T>C	NCBI36
NG_008838.2:g.216922A>G
NG_008838.3:g.216970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6276A>G MANE Select	ENSP00000362441.4:p.Ala2092=
ENST00000675732.1:c.1374A>G	ENSP00000502598.1:p.Ala458=
ENST00000373344.9:c.6276A>G	ENSP00000362441.4:p.Ala2092=
ENST00000395603.7:c.6162A>G	ENSP00000378967.3:p.Ala2054=
ENST00000480283.5:c.*5904A>G	ENSP00000480196.1:n.*5904A>G
ENST00000623316.1:c.760A>G
ENST00000623706.3:n.3346A>G
NM_000489.4:c.6276A>G	NP_000480.3:p.Ala2092=
NM_138270.3:c.6162A>G	NP_612114.2:p.Ala2054=
XM_005262153.3:c.6273A>G	XP_005262210.2:p.Ala2091=
XM_005262154.3:c.6189A>G	XP_005262211.2:p.Ala2063=
XM_005262155.3:c.6159A>G	XP_005262212.2:p.Ala2053=
XM_005262156.3:c.6111A>G	XP_005262213.2:p.Ala2037=
XM_005262157.3:c.6072A>G	XP_005262214.2:p.Ala2024=
XM_006724666.2:c.6159A>G	XP_006724729.1:p.Ala2053=
XM_006724667.2:c.5997A>G	XP_006724730.1:p.Ala1999=
XR_938400.1:n.6618A>G
NM_000489.5:c.6276A>G	NP_000480.3:p.Ala2092=
XM_005262153.5:c.6273A>G	XP_005262210.2:p.Ala2091=
XM_005262154.5:c.6189A>G	XP_005262211.2:p.Ala2063=
XM_005262155.4:c.6159A>G	XP_005262212.2:p.Ala2053=
XM_005262156.4:c.6111A>G	XP_005262213.2:p.Ala2037=
XM_005262157.5:c.6072A>G	XP_005262214.2:p.Ala2024=
XM_006724666.4:c.6159A>G	XP_006724729.1:p.Ala2053=
XM_006724667.3:c.5997A>G	XP_006724730.1:p.Ala1999=
XM_017029601.2:c.6186A>G	XP_016885090.1:p.Ala2062=
XM_017029602.1:c.6156A>G	XP_016885091.1:p.Ala2052=
XM_017029603.1:c.6108A>G	XP_016885092.1:p.Ala2036=
XM_017029604.2:c.6075A>G	XP_016885093.1:p.Ala2025=
XM_017029605.1:c.6072A>G	XP_016885094.1:p.Ala2024=
XM_017029606.2:c.6045A>G	XP_016885095.1:p.Ala2015=
XM_017029607.2:c.6042A>G	XP_016885096.1:p.Ala2014=
XM_017029608.2:c.5994A>G	XP_016885097.1:p.Ala1998=
XM_017029609.1:c.5958A>G	XP_016885098.1:p.Ala1986=
XM_017029610.1:c.5955A>G	XP_016885099.1:p.Ala1985=
XM_017029611.1:c.5910A>G	XP_016885100.1:p.Ala1970=
XR_001755700.2:n.6575A>G
NM_138270.4:c.6162A>G	NP_612114.2:p.Ala2054=
NM_000489.6:c.6276A>G MANE Select	NP_000480.3:p.Ala2092=
NM_138270.5:c.6162A>G	NP_612114.2:p.Ala2054=