Canonical Allele Identifier: CA517374764

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76829750C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77574285C>T , CM000685.2:g.77574285C>T	GRCh38
NC_000023.10:g.76829750C>T , CM000685.1:g.76829750C>T	GRCh37
NC_000023.9:g.76716406C>T	NCBI36
NG_008838.2:g.216937G>A
NG_008838.3:g.216985G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6291G>A MANE Select	ENSP00000362441.4:p.Lys2097=
ENST00000675732.1:c.1389G>A	ENSP00000502598.1:p.Lys463=
ENST00000373344.9:c.6291G>A	ENSP00000362441.4:p.Lys2097=
ENST00000395603.7:c.6177G>A	ENSP00000378967.3:p.Lys2059=
ENST00000480283.5:c.*5919G>A	ENSP00000480196.1:n.*5919G>A
ENST00000623316.1:c.775G>A
ENST00000623706.3:n.3361G>A
NM_000489.4:c.6291G>A	NP_000480.3:p.Lys2097=
NM_138270.3:c.6177G>A	NP_612114.2:p.Lys2059=
XM_005262153.3:c.6288G>A	XP_005262210.2:p.Lys2096=
XM_005262154.3:c.6204G>A	XP_005262211.2:p.Lys2068=
XM_005262155.3:c.6174G>A	XP_005262212.2:p.Lys2058=
XM_005262156.3:c.6126G>A	XP_005262213.2:p.Lys2042=
XM_005262157.3:c.6087G>A	XP_005262214.2:p.Lys2029=
XM_006724666.2:c.6174G>A	XP_006724729.1:p.Lys2058=
XM_006724667.2:c.6012G>A	XP_006724730.1:p.Lys2004=
XR_938400.1:n.6633G>A
NM_000489.5:c.6291G>A	NP_000480.3:p.Lys2097=
XM_005262153.5:c.6288G>A	XP_005262210.2:p.Lys2096=
XM_005262154.5:c.6204G>A	XP_005262211.2:p.Lys2068=
XM_005262155.4:c.6174G>A	XP_005262212.2:p.Lys2058=
XM_005262156.4:c.6126G>A	XP_005262213.2:p.Lys2042=
XM_005262157.5:c.6087G>A	XP_005262214.2:p.Lys2029=
XM_006724666.4:c.6174G>A	XP_006724729.1:p.Lys2058=
XM_006724667.3:c.6012G>A	XP_006724730.1:p.Lys2004=
XM_017029601.2:c.6201G>A	XP_016885090.1:p.Lys2067=
XM_017029602.1:c.6171G>A	XP_016885091.1:p.Lys2057=
XM_017029603.1:c.6123G>A	XP_016885092.1:p.Lys2041=
XM_017029604.2:c.6090G>A	XP_016885093.1:p.Lys2030=
XM_017029605.1:c.6087G>A	XP_016885094.1:p.Lys2029=
XM_017029606.2:c.6060G>A	XP_016885095.1:p.Lys2020=
XM_017029607.2:c.6057G>A	XP_016885096.1:p.Lys2019=
XM_017029608.2:c.6009G>A	XP_016885097.1:p.Lys2003=
XM_017029609.1:c.5973G>A	XP_016885098.1:p.Lys1991=
XM_017029610.1:c.5970G>A	XP_016885099.1:p.Lys1990=
XM_017029611.1:c.5925G>A	XP_016885100.1:p.Lys1975=
XR_001755700.2:n.6590G>A
NM_138270.4:c.6177G>A	NP_612114.2:p.Lys2059=
NM_000489.6:c.6291G>A MANE Select	NP_000480.3:p.Lys2097=
NM_138270.5:c.6177G>A	NP_612114.2:p.Lys2059=