Canonical Allele Identifier: CA517373965

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763847G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508369G>C , CM000685.2:g.77508369G>C	GRCh38
NC_000023.10:g.76763847G>C , CM000685.1:g.76763847G>C	GRCh37
NC_000023.9:g.76650503G>C	NCBI36
NG_008838.2:g.282853C>G
NG_008838.3:g.282901C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7461C>G MANE Select	ENSP00000362441.4:p.Ser2487=
ENST00000675732.1:c.2559C>G	ENSP00000502598.1:p.Ser853=
ENST00000373344.9:c.7461C>G	ENSP00000362441.4:p.Ser2487=
ENST00000395603.7:c.7347C>G	ENSP00000378967.3:p.Ser2449=
ENST00000480283.5:c.*7089C>G	ENSP00000480196.1:n.*7089C>G
ENST00000623706.3:n.5781C>G
NM_000489.4:c.7461C>G	NP_000480.3:p.Ser2487=
NM_138270.3:c.7347C>G	NP_612114.2:p.Ser2449=
XM_005262153.3:c.7458C>G	XP_005262210.2:p.Ser2486=
XM_005262154.3:c.7374C>G	XP_005262211.2:p.Ser2458=
XM_005262155.3:c.7344C>G	XP_005262212.2:p.Ser2448=
XM_005262156.3:c.7296C>G	XP_005262213.2:p.Ser2432=
XM_005262157.3:c.7257C>G	XP_005262214.2:p.Ser2419=
XM_006724666.2:c.7344C>G	XP_006724729.1:p.Ser2448=
XM_006724667.2:c.7182C>G	XP_006724730.1:p.Ser2394=
XR_938400.1:n.9053C>G
NM_000489.5:c.7461C>G	NP_000480.3:p.Ser2487=
XM_005262153.5:c.7458C>G	XP_005262210.2:p.Ser2486=
XM_005262154.5:c.7374C>G	XP_005262211.2:p.Ser2458=
XM_005262155.4:c.7344C>G	XP_005262212.2:p.Ser2448=
XM_005262156.4:c.7296C>G	XP_005262213.2:p.Ser2432=
XM_005262157.5:c.7257C>G	XP_005262214.2:p.Ser2419=
XM_006724666.4:c.7344C>G	XP_006724729.1:p.Ser2448=
XM_006724667.3:c.7182C>G	XP_006724730.1:p.Ser2394=
XM_017029601.2:c.7371C>G	XP_016885090.1:p.Ser2457=
XM_017029602.1:c.7341C>G	XP_016885091.1:p.Ser2447=
XM_017029603.1:c.7293C>G	XP_016885092.1:p.Ser2431=
XM_017029604.2:c.7260C>G	XP_016885093.1:p.Ser2420=
XM_017029605.1:c.7257C>G	XP_016885094.1:p.Ser2419=
XM_017029606.2:c.7230C>G	XP_016885095.1:p.Ser2410=
XM_017029607.2:c.7227C>G	XP_016885096.1:p.Ser2409=
XM_017029608.2:c.7179C>G	XP_016885097.1:p.Ser2393=
XM_017029609.1:c.7143C>G	XP_016885098.1:p.Ser2381=
XM_017029610.1:c.7140C>G	XP_016885099.1:p.Ser2380=
XM_017029611.1:c.7095C>G	XP_016885100.1:p.Ser2365=
XR_001755700.2:n.7760C>G
NM_138270.4:c.7347C>G	NP_612114.2:p.Ser2449=
NM_000489.6:c.7461C>G MANE Select	NP_000480.3:p.Ser2487=
NM_138270.5:c.7347C>G	NP_612114.2:p.Ser2449=