Canonical Allele Identifier: CA413704278

Gene: ATRX

Linked Data

• dbSNP Id: rs2147648991
• MyVariant Identifiers: chrX:g.76763966G>C (hg19) ; chrX:g.77508488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508488G>C , CM000685.2:g.77508488G>C	GRCh38
NC_000023.10:g.76763966G>C , CM000685.1:g.76763966G>C	GRCh37
NC_000023.9:g.76650622G>C	NCBI36
NG_008838.2:g.282734C>G
NG_008838.3:g.282782C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7342C>G MANE Select	ENSP00000362441.4:p.Pro2448Ala
ENST00000675732.1:c.2440C>G	ENSP00000502598.1:p.Pro814Ala
ENST00000373344.9:c.7342C>G	ENSP00000362441.4:p.Pro2448Ala
ENST00000395603.7:c.7228C>G	ENSP00000378967.3:p.Pro2410Ala
ENST00000480283.5:c.*6970C>G	ENSP00000480196.1:n.*6970C>G
ENST00000623706.3:n.5662C>G
ENST00000624766.1:n.573C>G
NM_000489.4:c.7342C>G	NP_000480.3:p.Pro2448Ala
NM_138270.3:c.7228C>G	NP_612114.2:p.Pro2410Ala
XM_005262153.3:c.7339C>G	XP_005262210.2:p.Pro2447Ala
XM_005262154.3:c.7255C>G	XP_005262211.2:p.Pro2419Ala
XM_005262155.3:c.7225C>G	XP_005262212.2:p.Pro2409Ala
XM_005262156.3:c.7177C>G	XP_005262213.2:p.Pro2393Ala
XM_005262157.3:c.7138C>G	XP_005262214.2:p.Pro2380Ala
XM_006724666.2:c.7225C>G	XP_006724729.1:p.Pro2409Ala
XM_006724667.2:c.7063C>G	XP_006724730.1:p.Pro2355Ala
XR_938400.1:n.8934C>G
NM_000489.5:c.7342C>G	NP_000480.3:p.Pro2448Ala
XM_005262153.5:c.7339C>G	XP_005262210.2:p.Pro2447Ala
XM_005262154.5:c.7255C>G	XP_005262211.2:p.Pro2419Ala
XM_005262155.4:c.7225C>G	XP_005262212.2:p.Pro2409Ala
XM_005262156.4:c.7177C>G	XP_005262213.2:p.Pro2393Ala
XM_005262157.5:c.7138C>G	XP_005262214.2:p.Pro2380Ala
XM_006724666.4:c.7225C>G	XP_006724729.1:p.Pro2409Ala
XM_006724667.3:c.7063C>G	XP_006724730.1:p.Pro2355Ala
XM_017029601.2:c.7252C>G	XP_016885090.1:p.Pro2418Ala
XM_017029602.1:c.7222C>G	XP_016885091.1:p.Pro2408Ala
XM_017029603.1:c.7174C>G	XP_016885092.1:p.Pro2392Ala
XM_017029604.2:c.7141C>G	XP_016885093.1:p.Pro2381Ala
XM_017029605.1:c.7138C>G	XP_016885094.1:p.Pro2380Ala
XM_017029606.2:c.7111C>G	XP_016885095.1:p.Pro2371Ala
XM_017029607.2:c.7108C>G	XP_016885096.1:p.Pro2370Ala
XM_017029608.2:c.7060C>G	XP_016885097.1:p.Pro2354Ala
XM_017029609.1:c.7024C>G	XP_016885098.1:p.Pro2342Ala
XM_017029610.1:c.7021C>G	XP_016885099.1:p.Pro2341Ala
XM_017029611.1:c.6976C>G	XP_016885100.1:p.Pro2326Ala
XR_001755700.2:n.7641C>G
NM_138270.4:c.7228C>G	NP_612114.2:p.Pro2410Ala
NM_000489.6:c.7342C>G MANE Select	NP_000480.3:p.Pro2448Ala
NM_138270.5:c.7228C>G	NP_612114.2:p.Pro2410Ala