Canonical Allele Identifier: CA413705515

Gene: ATRX

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77634704C>G , CM000685.2:g.77634704C>G	GRCh38
NC_000023.10:g.76890195C>G , CM000685.1:g.76890195C>G	GRCh37
NC_000023.9:g.76776851C>G	NCBI36
NG_008838.2:g.156518G>C
NG_008838.3:g.156566G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.4700-1G>C MANE Select	ENSP00000362441.4:n.4700-1G>C
ENST00000373344.9:c.4700-1G>C	ENSP00000362441.4:n.4700-1G>C
ENST00000395603.7:c.4586-1G>C	ENSP00000378967.3:n.4586-1G>C
ENST00000460639.2:n.180-1G>C
ENST00000480283.5:c.*4328-1G>C	ENSP00000480196.1:n.*4328-1G>C
ENST00000623242.3:c.437-1G>C
NM_000489.4:c.4700-1G>C	NP_000480.3:n.4700-1G>C
NM_138270.3:c.4586-1G>C	NP_612114.2:n.4586-1G>C
XM_005262153.3:c.4697-1G>C	XP_005262210.2:n.4697-1G>C
XM_005262154.3:c.4613-1G>C	XP_005262211.2:n.4613-1G>C
XM_005262155.3:c.4583-1G>C	XP_005262212.2:n.4583-1G>C
XM_005262156.3:c.4535-1G>C	XP_005262213.2:n.4535-1G>C
XM_005262157.3:c.4496-1G>C	XP_005262214.2:n.4496-1G>C
XM_006724666.2:c.4583-1G>C	XP_006724729.1:n.4583-1G>C
XM_006724667.2:c.4421-1G>C	XP_006724730.1:n.4421-1G>C
XM_006724668.2:c.4700-1G>C	XP_006724731.1:n.4700-1G>C
XR_938400.1:n.4968-1G>C
NM_000489.5:c.4700-1G>C	NP_000480.3:n.4700-1G>C
XM_005262153.5:c.4697-1G>C	XP_005262210.2:n.4697-1G>C
XM_005262154.5:c.4613-1G>C	XP_005262211.2:n.4613-1G>C
XM_005262155.4:c.4583-1G>C	XP_005262212.2:n.4583-1G>C
XM_005262156.4:c.4535-1G>C	XP_005262213.2:n.4535-1G>C
XM_005262157.5:c.4496-1G>C	XP_005262214.2:n.4496-1G>C
XM_006724666.4:c.4583-1G>C	XP_006724729.1:n.4583-1G>C
XM_006724667.3:c.4421-1G>C	XP_006724730.1:n.4421-1G>C
XM_006724668.3:c.4700-1G>C	XP_006724731.1:n.4700-1G>C
XM_017029601.2:c.4610-1G>C	XP_016885090.1:n.4610-1G>C
XM_017029602.1:c.4580-1G>C	XP_016885091.1:n.4580-1G>C
XM_017029603.1:c.4532-1G>C	XP_016885092.1:n.4532-1G>C
XM_017029604.2:c.4499-1G>C	XP_016885093.1:n.4499-1G>C
XM_017029605.1:c.4496-1G>C	XP_016885094.1:n.4496-1G>C
XM_017029606.2:c.4469-1G>C	XP_016885095.1:n.4469-1G>C
XM_017029607.2:c.4466-1G>C	XP_016885096.1:n.4466-1G>C
XM_017029608.2:c.4418-1G>C	XP_016885097.1:n.4418-1G>C
XM_017029609.1:c.4382-1G>C	XP_016885098.1:n.4382-1G>C
XM_017029610.1:c.4379-1G>C	XP_016885099.1:n.4379-1G>C
XM_017029611.1:c.4334-1G>C	XP_016885100.1:n.4334-1G>C
XR_001755700.2:n.4925-1G>C
NM_138270.4:c.4586-1G>C	NP_612114.2:n.4586-1G>C
NM_000489.6:c.4700-1G>C MANE Select	NP_000480.3:n.4700-1G>C
NM_138270.5:c.4586-1G>C	NP_612114.2:n.4586-1G>C