Canonical Allele Identifier: CA517373977

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763856T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508378T>A , CM000685.2:g.77508378T>A	GRCh38
NC_000023.10:g.76763856T>A , CM000685.1:g.76763856T>A	GRCh37
NC_000023.9:g.76650512T>A	NCBI36
NG_008838.2:g.282844A>T
NG_008838.3:g.282892A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373344.11:c.7452A>T MANE Select	ENSP00000362441.4:p.Pro2484=
ENST00000675732.1:c.2550A>T	ENSP00000502598.1:p.Pro850=
ENST00000373344.9:c.7452A>T	ENSP00000362441.4:p.Pro2484=
ENST00000395603.7:c.7338A>T	ENSP00000378967.3:p.Pro2446=
ENST00000480283.5:c.*7080A>T	ENSP00000480196.1:n.*7080A>T
ENST00000623706.3:n.5772A>T
NM_000489.4:c.7452A>T	NP_000480.3:p.Pro2484=
NM_138270.3:c.7338A>T	NP_612114.2:p.Pro2446=
XM_005262153.3:c.7449A>T	XP_005262210.2:p.Pro2483=
XM_005262154.3:c.7365A>T	XP_005262211.2:p.Pro2455=
XM_005262155.3:c.7335A>T	XP_005262212.2:p.Pro2445=
XM_005262156.3:c.7287A>T	XP_005262213.2:p.Pro2429=
XM_005262157.3:c.7248A>T	XP_005262214.2:p.Pro2416=
XM_006724666.2:c.7335A>T	XP_006724729.1:p.Pro2445=
XM_006724667.2:c.7173A>T	XP_006724730.1:p.Pro2391=
XR_938400.1:n.9044A>T
NM_000489.5:c.7452A>T	NP_000480.3:p.Pro2484=
XM_005262153.5:c.7449A>T	XP_005262210.2:p.Pro2483=
XM_005262154.5:c.7365A>T	XP_005262211.2:p.Pro2455=
XM_005262155.4:c.7335A>T	XP_005262212.2:p.Pro2445=
XM_005262156.4:c.7287A>T	XP_005262213.2:p.Pro2429=
XM_005262157.5:c.7248A>T	XP_005262214.2:p.Pro2416=
XM_006724666.4:c.7335A>T	XP_006724729.1:p.Pro2445=
XM_006724667.3:c.7173A>T	XP_006724730.1:p.Pro2391=
XM_017029601.2:c.7362A>T	XP_016885090.1:p.Pro2454=
XM_017029602.1:c.7332A>T	XP_016885091.1:p.Pro2444=
XM_017029603.1:c.7284A>T	XP_016885092.1:p.Pro2428=
XM_017029604.2:c.7251A>T	XP_016885093.1:p.Pro2417=
XM_017029605.1:c.7248A>T	XP_016885094.1:p.Pro2416=
XM_017029606.2:c.7221A>T	XP_016885095.1:p.Pro2407=
XM_017029607.2:c.7218A>T	XP_016885096.1:p.Pro2406=
XM_017029608.2:c.7170A>T	XP_016885097.1:p.Pro2390=
XM_017029609.1:c.7134A>T	XP_016885098.1:p.Pro2378=
XM_017029610.1:c.7131A>T	XP_016885099.1:p.Pro2377=
XM_017029611.1:c.7086A>T	XP_016885100.1:p.Pro2362=
XR_001755700.2:n.7751A>T
NM_138270.4:c.7338A>T	NP_612114.2:p.Pro2446=
NM_000489.6:c.7452A>T MANE Select	NP_000480.3:p.Pro2484=
NM_138270.5:c.7338A>T	NP_612114.2:p.Pro2446=