Canonical Allele Identifier: CA413704413

Gene: ATRX

Linked Data

• MyVariant Identifiers: chrX:g.76763981T>G (hg19) ; chrX:g.77508503T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508503T>G , CM000685.2:g.77508503T>G	GRCh38
NC_000023.10:g.76763981T>G , CM000685.1:g.76763981T>G	GRCh37
NC_000023.9:g.76650637T>G	NCBI36
NG_008838.2:g.282719A>C
NG_008838.3:g.282767A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7327A>C MANE Select	ENSP00000362441.4:p.Asn2443His
ENST00000675732.1:c.2425A>C	ENSP00000502598.1:p.Asn809His
ENST00000373344.9:c.7327A>C	ENSP00000362441.4:p.Asn2443His
ENST00000395603.7:c.7213A>C	ENSP00000378967.3:p.Asn2405His
ENST00000480283.5:c.*6955A>C	ENSP00000480196.1:n.*6955A>C
ENST00000623706.3:n.5647A>C
ENST00000624766.1:n.558A>C
NM_000489.4:c.7327A>C	NP_000480.3:p.Asn2443His
NM_138270.3:c.7213A>C	NP_612114.2:p.Asn2405His
XM_005262153.3:c.7324A>C	XP_005262210.2:p.Asn2442His
XM_005262154.3:c.7240A>C	XP_005262211.2:p.Asn2414His
XM_005262155.3:c.7210A>C	XP_005262212.2:p.Asn2404His
XM_005262156.3:c.7162A>C	XP_005262213.2:p.Asn2388His
XM_005262157.3:c.7123A>C	XP_005262214.2:p.Asn2375His
XM_006724666.2:c.7210A>C	XP_006724729.1:p.Asn2404His
XM_006724667.2:c.7048A>C	XP_006724730.1:p.Asn2350His
XR_938400.1:n.8919A>C
NM_000489.5:c.7327A>C	NP_000480.3:p.Asn2443His
XM_005262153.5:c.7324A>C	XP_005262210.2:p.Asn2442His
XM_005262154.5:c.7240A>C	XP_005262211.2:p.Asn2414His
XM_005262155.4:c.7210A>C	XP_005262212.2:p.Asn2404His
XM_005262156.4:c.7162A>C	XP_005262213.2:p.Asn2388His
XM_005262157.5:c.7123A>C	XP_005262214.2:p.Asn2375His
XM_006724666.4:c.7210A>C	XP_006724729.1:p.Asn2404His
XM_006724667.3:c.7048A>C	XP_006724730.1:p.Asn2350His
XM_017029601.2:c.7237A>C	XP_016885090.1:p.Asn2413His
XM_017029602.1:c.7207A>C	XP_016885091.1:p.Asn2403His
XM_017029603.1:c.7159A>C	XP_016885092.1:p.Asn2387His
XM_017029604.2:c.7126A>C	XP_016885093.1:p.Asn2376His
XM_017029605.1:c.7123A>C	XP_016885094.1:p.Asn2375His
XM_017029606.2:c.7096A>C	XP_016885095.1:p.Asn2366His
XM_017029607.2:c.7093A>C	XP_016885096.1:p.Asn2365His
XM_017029608.2:c.7045A>C	XP_016885097.1:p.Asn2349His
XM_017029609.1:c.7009A>C	XP_016885098.1:p.Asn2337His
XM_017029610.1:c.7006A>C	XP_016885099.1:p.Asn2336His
XM_017029611.1:c.6961A>C	XP_016885100.1:p.Asn2321His
XR_001755700.2:n.7626A>C
NM_138270.4:c.7213A>C	NP_612114.2:p.Asn2405His
NM_000489.6:c.7327A>C MANE Select	NP_000480.3:p.Asn2443His
NM_138270.5:c.7213A>C	NP_612114.2:p.Asn2405His