Canonical Allele Identifier: CA2694140501

Gene: ATRX

Linked Data

• gnomAD v4: X-77589825-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77589825G>A , CM000685.2:g.77589825G>A	GRCh38
NC_000023.10:g.76845295G>A , CM000685.1:g.76845295G>A	GRCh37
NC_000023.9:g.76731951G>A	NCBI36
NG_008838.2:g.201397C>T
NG_008838.3:g.201445C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.6217+9C>T MANE Select	ENSP00000362441.4:n.6217+9C>T
ENST00000636868.1:n.39+9C>T
ENST00000675732.1:c.1315+9C>T	ENSP00000502598.1:n.1315+9C>T
ENST00000373344.9:c.6217+9C>T	ENSP00000362441.4:n.6217+9C>T
ENST00000395603.7:c.6103+9C>T	ENSP00000378967.3:n.6103+9C>T
ENST00000480283.5:c.*5845+9C>T	ENSP00000480196.1:n.*5845+9C>T
ENST00000623316.1:c.701+9C>T
ENST00000623706.3:n.3287+9C>T
NM_000489.4:c.6217+9C>T	NP_000480.3:n.6217+9C>T
NM_138270.3:c.6103+9C>T	NP_612114.2:n.6103+9C>T
XM_005262153.3:c.6214+9C>T	XP_005262210.2:n.6214+9C>T
XM_005262154.3:c.6130+9C>T	XP_005262211.2:n.6130+9C>T
XM_005262155.3:c.6100+9C>T	XP_005262212.2:n.6100+9C>T
XM_005262156.3:c.6052+9C>T	XP_005262213.2:n.6052+9C>T
XM_005262157.3:c.6013+9C>T	XP_005262214.2:n.6013+9C>T
XM_006724666.2:c.6100+9C>T	XP_006724729.1:n.6100+9C>T
XM_006724667.2:c.5938+9C>T	XP_006724730.1:n.5938+9C>T
XR_938400.1:n.6559+9C>T
NM_000489.5:c.6217+9C>T	NP_000480.3:n.6217+9C>T
XM_005262153.5:c.6214+9C>T	XP_005262210.2:n.6214+9C>T
XM_005262154.5:c.6130+9C>T	XP_005262211.2:n.6130+9C>T
XM_005262155.4:c.6100+9C>T	XP_005262212.2:n.6100+9C>T
XM_005262156.4:c.6052+9C>T	XP_005262213.2:n.6052+9C>T
XM_005262157.5:c.6013+9C>T	XP_005262214.2:n.6013+9C>T
XM_006724666.4:c.6100+9C>T	XP_006724729.1:n.6100+9C>T
XM_006724667.3:c.5938+9C>T	XP_006724730.1:n.5938+9C>T
XM_017029601.2:c.6127+9C>T	XP_016885090.1:n.6127+9C>T
XM_017029602.1:c.6097+9C>T	XP_016885091.1:n.6097+9C>T
XM_017029603.1:c.6049+9C>T	XP_016885092.1:n.6049+9C>T
XM_017029604.2:c.6016+9C>T	XP_016885093.1:n.6016+9C>T
XM_017029605.1:c.6013+9C>T	XP_016885094.1:n.6013+9C>T
XM_017029606.2:c.5986+9C>T	XP_016885095.1:n.5986+9C>T
XM_017029607.2:c.5983+9C>T	XP_016885096.1:n.5983+9C>T
XM_017029608.2:c.5935+9C>T	XP_016885097.1:n.5935+9C>T
XM_017029609.1:c.5899+9C>T	XP_016885098.1:n.5899+9C>T
XM_017029610.1:c.5896+9C>T	XP_016885099.1:n.5896+9C>T
XM_017029611.1:c.5851+9C>T	XP_016885100.1:n.5851+9C>T
XR_001755700.2:n.6516+9C>T
NM_138270.4:c.6103+9C>T	NP_612114.2:n.6103+9C>T
NM_000489.6:c.6217+9C>T MANE Select	NP_000480.3:n.6217+9C>T
NM_138270.5:c.6103+9C>T	NP_612114.2:n.6103+9C>T