Canonical Allele Identifier: CA10458408

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77785986T>C , CM000685.2:g.77785986T>C	GRCh38
NC_000023.10:g.77041472T>C , CM000685.1:g.77041472T>C	GRCh37
NC_000023.9:g.76928128T>C	NCBI36
NG_008838.2:g.5236A>G
NG_008838.3:g.5284A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000489.6:c.16A>G MANE Select	NP_000480.3:p.Met6Val
ENST00000373344.11:c.16A>G MANE Select	ENSP00000362441.4:p.Met6Val
NM_000489.4:c.16A>G	NP_000480.3:p.Met6Val
NM_000489.5:c.16A>G	NP_000480.3:p.Met6Val
NM_138270.3:c.16A>G	NP_612114.2:p.Met6Val
NM_138270.4:c.16A>G	NP_612114.2:p.Met6Val
NM_138270.5:c.16A>G	NP_612114.2:p.Met6Val
ENST00000373344.9:c.16A>G	ENSP00000362441.4:p.Met6Val
ENST00000395603.7:c.16A>G	ENSP00000378967.3:p.Met6Val
ENST00000480283.5:c.16A>G	ENSP00000480196.1:p.Met6Val
ENST00000622960.1:c.-239A>G	ENSP00000485587.1:n.-239A>G
ENST00000623321.3:c.-37A>G	ENSP00000485127.1:n.-37A>G
ENST00000624032.3:c.16A>G	ENSP00000485253.1:p.Met6Val
ENST00000624166.3:c.16A>G	ENSP00000485103.1:p.Met6Val
ENST00000624193.1:n.219A>G
ENST00000624668.3:c.-37A>G	ENSP00000485100.1:n.-37A>G
XM_005262153.3:c.16A>G	XP_005262210.2:p.Met6Val
XM_005262153.5:c.16A>G	XP_005262210.2:p.Met6Val
XM_005262154.3:c.16A>G	XP_005262211.2:p.Met6Val
XM_005262154.5:c.16A>G	XP_005262211.2:p.Met6Val
XM_005262155.3:c.-239A>G	XP_005262212.2:n.-239A>G
XM_005262155.4:c.-239A>G	XP_005262212.2:n.-239A>G
XM_005262156.3:c.-37A>G	XP_005262213.2:n.-37A>G
XM_005262156.4:c.-37A>G	XP_005262213.2:n.-37A>G
XM_005262157.3:c.16A>G	XP_005262214.2:p.Met6Val
XM_005262157.5:c.16A>G	XP_005262214.2:p.Met6Val
XM_006724666.2:c.16A>G	XP_006724729.1:p.Met6Val
XM_006724666.4:c.16A>G	XP_006724729.1:p.Met6Val
XM_006724667.2:c.-37A>G	XP_006724730.1:n.-37A>G
XM_006724667.3:c.-37A>G	XP_006724730.1:n.-37A>G
XM_006724668.2:c.16A>G	XP_006724731.1:p.Met6Val
XM_006724668.3:c.16A>G	XP_006724731.1:p.Met6Val
XM_017029601.2:c.16A>G	XP_016885090.1:p.Met6Val
XM_017029602.1:c.-239A>G	XP_016885091.1:n.-239A>G
XM_017029603.1:c.-37A>G	XP_016885092.1:n.-37A>G
XM_017029604.2:c.16A>G	XP_016885093.1:p.Met6Val
XM_017029605.1:c.-239A>G	XP_016885094.1:n.-239A>G
XM_017029606.2:c.-239A>G	XP_016885095.1:n.-239A>G
XM_017029607.2:c.-239A>G	XP_016885096.1:n.-239A>G
XM_017029608.2:c.-37A>G	XP_016885097.1:n.-37A>G
XM_017029609.1:c.-239A>G	XP_016885098.1:n.-239A>G
XM_017029610.1:c.-239A>G	XP_016885099.1:n.-239A>G
XM_017029611.1:c.-37A>G	XP_016885100.1:n.-37A>G
XR_001755700.2:n.241A>G
XR_938400.1:n.284A>G