Canonical Allele Identifier: CA2438929024

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508395T= , CM000685.2:g.77508395T=	GRCh38
NC_000023.10:g.76763873T= , CM000685.1:g.76763873T=	GRCh37
NC_000023.9:g.76650529T=	NCBI36
NG_008838.2:g.282827A=
NG_008838.3:g.282875A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7435A= MANE Select	ENSP00000362441.4:p.Met2479=
ENST00000675732.1:c.2533A=	ENSP00000502598.1:p.Met845=
ENST00000373344.9:c.7435A=	ENSP00000362441.4:p.Met2479=
ENST00000395603.7:c.7321A=	ENSP00000378967.3:p.Met2441=
ENST00000480283.5:c.*7063A=	ENSP00000480196.1:n.*7063A=
ENST00000623706.3:n.5755A=
NM_000489.4:c.7435A=	NP_000480.3:p.Met2479=
NM_138270.3:c.7321A=	NP_612114.2:p.Met2441=
XM_005262153.3:c.7432A=	XP_005262210.2:p.Met2478=
XM_005262154.3:c.7348A=	XP_005262211.2:p.Met2450=
XM_005262155.3:c.7318A=	XP_005262212.2:p.Met2440=
XM_005262156.3:c.7270A=	XP_005262213.2:p.Met2424=
XM_005262157.3:c.7231A=	XP_005262214.2:p.Met2411=
XM_006724666.2:c.7318A=	XP_006724729.1:p.Met2440=
XM_006724667.2:c.7156A=	XP_006724730.1:p.Met2386=
XR_938400.1:n.9027A=
NM_000489.5:c.7435A=	NP_000480.3:p.Met2479=
XM_005262153.5:c.7432A=	XP_005262210.2:p.Met2478=
XM_005262154.5:c.7348A=	XP_005262211.2:p.Met2450=
XM_005262155.4:c.7318A=	XP_005262212.2:p.Met2440=
XM_005262156.4:c.7270A=	XP_005262213.2:p.Met2424=
XM_005262157.5:c.7231A=	XP_005262214.2:p.Met2411=
XM_006724666.4:c.7318A=	XP_006724729.1:p.Met2440=
XM_006724667.3:c.7156A=	XP_006724730.1:p.Met2386=
XM_017029601.2:c.7345A=	XP_016885090.1:p.Met2449=
XM_017029602.1:c.7315A=	XP_016885091.1:p.Met2439=
XM_017029603.1:c.7267A=	XP_016885092.1:p.Met2423=
XM_017029604.2:c.7234A=	XP_016885093.1:p.Met2412=
XM_017029605.1:c.7231A=	XP_016885094.1:p.Met2411=
XM_017029606.2:c.7204A=	XP_016885095.1:p.Met2402=
XM_017029607.2:c.7201A=	XP_016885096.1:p.Met2401=
XM_017029608.2:c.7153A=	XP_016885097.1:p.Met2385=
XM_017029609.1:c.7117A=	XP_016885098.1:p.Met2373=
XM_017029610.1:c.7114A=	XP_016885099.1:p.Met2372=
XM_017029611.1:c.7069A=	XP_016885100.1:p.Met2357=
XR_001755700.2:n.7734A=
NM_138270.4:c.7321A=	NP_612114.2:p.Met2441=
NM_000489.6:c.7435A= MANE Select	NP_000480.3:p.Met2479=
NM_138270.5:c.7321A=	NP_612114.2:p.Met2441=