Canonical Allele Identifier: CA413704303

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763969T>C (hg19) ; chrX:g.77508491T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508491T>C , CM000685.2:g.77508491T>C	GRCh38
NC_000023.10:g.76763969T>C , CM000685.1:g.76763969T>C	GRCh37
NC_000023.9:g.76650625T>C	NCBI36
NG_008838.2:g.282731A>G
NG_008838.3:g.282779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7339A>G MANE Select	ENSP00000362441.4:p.Asn2447Asp
ENST00000675732.1:c.2437A>G	ENSP00000502598.1:p.Asn813Asp
ENST00000373344.9:c.7339A>G	ENSP00000362441.4:p.Asn2447Asp
ENST00000395603.7:c.7225A>G	ENSP00000378967.3:p.Asn2409Asp
ENST00000480283.5:c.*6967A>G	ENSP00000480196.1:n.*6967A>G
ENST00000623706.3:n.5659A>G
ENST00000624766.1:n.570A>G
NM_000489.4:c.7339A>G	NP_000480.3:p.Asn2447Asp
NM_138270.3:c.7225A>G	NP_612114.2:p.Asn2409Asp
XM_005262153.3:c.7336A>G	XP_005262210.2:p.Asn2446Asp
XM_005262154.3:c.7252A>G	XP_005262211.2:p.Asn2418Asp
XM_005262155.3:c.7222A>G	XP_005262212.2:p.Asn2408Asp
XM_005262156.3:c.7174A>G	XP_005262213.2:p.Asn2392Asp
XM_005262157.3:c.7135A>G	XP_005262214.2:p.Asn2379Asp
XM_006724666.2:c.7222A>G	XP_006724729.1:p.Asn2408Asp
XM_006724667.2:c.7060A>G	XP_006724730.1:p.Asn2354Asp
XR_938400.1:n.8931A>G
NM_000489.5:c.7339A>G	NP_000480.3:p.Asn2447Asp
XM_005262153.5:c.7336A>G	XP_005262210.2:p.Asn2446Asp
XM_005262154.5:c.7252A>G	XP_005262211.2:p.Asn2418Asp
XM_005262155.4:c.7222A>G	XP_005262212.2:p.Asn2408Asp
XM_005262156.4:c.7174A>G	XP_005262213.2:p.Asn2392Asp
XM_005262157.5:c.7135A>G	XP_005262214.2:p.Asn2379Asp
XM_006724666.4:c.7222A>G	XP_006724729.1:p.Asn2408Asp
XM_006724667.3:c.7060A>G	XP_006724730.1:p.Asn2354Asp
XM_017029601.2:c.7249A>G	XP_016885090.1:p.Asn2417Asp
XM_017029602.1:c.7219A>G	XP_016885091.1:p.Asn2407Asp
XM_017029603.1:c.7171A>G	XP_016885092.1:p.Asn2391Asp
XM_017029604.2:c.7138A>G	XP_016885093.1:p.Asn2380Asp
XM_017029605.1:c.7135A>G	XP_016885094.1:p.Asn2379Asp
XM_017029606.2:c.7108A>G	XP_016885095.1:p.Asn2370Asp
XM_017029607.2:c.7105A>G	XP_016885096.1:p.Asn2369Asp
XM_017029608.2:c.7057A>G	XP_016885097.1:p.Asn2353Asp
XM_017029609.1:c.7021A>G	XP_016885098.1:p.Asn2341Asp
XM_017029610.1:c.7018A>G	XP_016885099.1:p.Asn2340Asp
XM_017029611.1:c.6973A>G	XP_016885100.1:p.Asn2325Asp
XR_001755700.2:n.7638A>G
NM_138270.4:c.7225A>G	NP_612114.2:p.Asn2409Asp
NM_000489.6:c.7339A>G MANE Select	NP_000480.3:p.Asn2447Asp
NM_138270.5:c.7225A>G	NP_612114.2:p.Asn2409Asp