Canonical Allele Identifier: CA413707312

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76776355C>A (hg19) ; chrX:g.77520877C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77520877C>A , CM000685.2:g.77520877C>A	GRCh38
NC_000023.10:g.76776355C>A , CM000685.1:g.76776355C>A	GRCh37
NC_000023.9:g.76663011C>A	NCBI36
NG_008838.2:g.270345G>T
NG_008838.3:g.270393G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7111G>T MANE Select	ENSP00000362441.4:p.Ala2371Ser
ENST00000675732.1:c.2209G>T	ENSP00000502598.1:p.Ala737Ser
ENST00000373344.9:c.7111G>T	ENSP00000362441.4:p.Ala2371Ser
ENST00000395603.7:c.6997G>T	ENSP00000378967.3:p.Ala2333Ser
ENST00000480283.5:c.*6739G>T	ENSP00000480196.1:n.*6739G>T
ENST00000623706.3:n.5431G>T
ENST00000624766.1:n.342G>T
NM_000489.4:c.7111G>T	NP_000480.3:p.Ala2371Ser
NM_138270.3:c.6997G>T	NP_612114.2:p.Ala2333Ser
XM_005262153.3:c.7108G>T	XP_005262210.2:p.Ala2370Ser
XM_005262154.3:c.7024G>T	XP_005262211.2:p.Ala2342Ser
XM_005262155.3:c.6994G>T	XP_005262212.2:p.Ala2332Ser
XM_005262156.3:c.6946G>T	XP_005262213.2:p.Ala2316Ser
XM_005262157.3:c.6907G>T	XP_005262214.2:p.Ala2303Ser
XM_006724666.2:c.6994G>T	XP_006724729.1:p.Ala2332Ser
XM_006724667.2:c.6832G>T	XP_006724730.1:p.Ala2278Ser
XR_938400.1:n.8703G>T
NM_000489.5:c.7111G>T	NP_000480.3:p.Ala2371Ser
XM_005262153.5:c.7108G>T	XP_005262210.2:p.Ala2370Ser
XM_005262154.5:c.7024G>T	XP_005262211.2:p.Ala2342Ser
XM_005262155.4:c.6994G>T	XP_005262212.2:p.Ala2332Ser
XM_005262156.4:c.6946G>T	XP_005262213.2:p.Ala2316Ser
XM_005262157.5:c.6907G>T	XP_005262214.2:p.Ala2303Ser
XM_006724666.4:c.6994G>T	XP_006724729.1:p.Ala2332Ser
XM_006724667.3:c.6832G>T	XP_006724730.1:p.Ala2278Ser
XM_017029601.2:c.7021G>T	XP_016885090.1:p.Ala2341Ser
XM_017029602.1:c.6991G>T	XP_016885091.1:p.Ala2331Ser
XM_017029603.1:c.6943G>T	XP_016885092.1:p.Ala2315Ser
XM_017029604.2:c.6910G>T	XP_016885093.1:p.Ala2304Ser
XM_017029605.1:c.6907G>T	XP_016885094.1:p.Ala2303Ser
XM_017029606.2:c.6880G>T	XP_016885095.1:p.Ala2294Ser
XM_017029607.2:c.6877G>T	XP_016885096.1:p.Ala2293Ser
XM_017029608.2:c.6829G>T	XP_016885097.1:p.Ala2277Ser
XM_017029609.1:c.6793G>T	XP_016885098.1:p.Ala2265Ser
XM_017029610.1:c.6790G>T	XP_016885099.1:p.Ala2264Ser
XM_017029611.1:c.6745G>T	XP_016885100.1:p.Ala2249Ser
XR_001755700.2:n.7410G>T
NM_138270.4:c.6997G>T	NP_612114.2:p.Ala2333Ser
NM_000489.6:c.7111G>T MANE Select	NP_000480.3:p.Ala2371Ser
NM_138270.5:c.6997G>T	NP_612114.2:p.Ala2333Ser