Canonical Allele Identifier: CA2438929047

Gene: ATRX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.77508462_77508464delinsCAT , CM000685.2:g.77508462_77508464delinsCAT	GRCh38
NC_000023.10:g.76763940_76763942delinsCAT , CM000685.1:g.76763940_76763942delinsCAT	GRCh37
NC_000023.9:g.76650596_76650598delinsCAT	NCBI36
NG_008838.2:g.282758_282760delinsATG
NG_008838.3:g.282806_282808delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373344.11:c.7366_7368delinsATG MANE Select	ENSP00000362441.4:p.Met2456=
ENST00000675732.1:c.2464_2466delinsATG	ENSP00000502598.1:p.Met822=
ENST00000373344.9:c.7366_7368delinsATG	ENSP00000362441.4:p.Met2456=
ENST00000395603.7:c.7252_7254delinsATG	ENSP00000378967.3:p.Met2418=
ENST00000480283.5:c.*6994_*6996delinsATG	ENSP00000480196.1:n.*6994_*6996delinsATG
ENST00000623706.3:n.5686_5688delinsATG
NM_000489.4:c.7366_7368delinsATG	NP_000480.3:p.Met2456=
NM_138270.3:c.7252_7254delinsATG	NP_612114.2:p.Met2418=
XM_005262153.3:c.7363_7365delinsATG	XP_005262210.2:p.Met2455=
XM_005262154.3:c.7279_7281delinsATG	XP_005262211.2:p.Met2427=
XM_005262155.3:c.7249_7251delinsATG	XP_005262212.2:p.Met2417=
XM_005262156.3:c.7201_7203delinsATG	XP_005262213.2:p.Met2401=
XM_005262157.3:c.7162_7164delinsATG	XP_005262214.2:p.Met2388=
XM_006724666.2:c.7249_7251delinsATG	XP_006724729.1:p.Met2417=
XM_006724667.2:c.7087_7089delinsATG	XP_006724730.1:p.Met2363=
XR_938400.1:n.8958_8960delinsATG
NM_000489.5:c.7366_7368delinsATG	NP_000480.3:p.Met2456=
XM_005262153.5:c.7363_7365delinsATG	XP_005262210.2:p.Met2455=
XM_005262154.5:c.7279_7281delinsATG	XP_005262211.2:p.Met2427=
XM_005262155.4:c.7249_7251delinsATG	XP_005262212.2:p.Met2417=
XM_005262156.4:c.7201_7203delinsATG	XP_005262213.2:p.Met2401=
XM_005262157.5:c.7162_7164delinsATG	XP_005262214.2:p.Met2388=
XM_006724666.4:c.7249_7251delinsATG	XP_006724729.1:p.Met2417=
XM_006724667.3:c.7087_7089delinsATG	XP_006724730.1:p.Met2363=
XM_017029601.2:c.7276_7278delinsATG	XP_016885090.1:p.Met2426=
XM_017029602.1:c.7246_7248delinsATG	XP_016885091.1:p.Met2416=
XM_017029603.1:c.7198_7200delinsATG	XP_016885092.1:p.Met2400=
XM_017029604.2:c.7165_7167delinsATG	XP_016885093.1:p.Met2389=
XM_017029605.1:c.7162_7164delinsATG	XP_016885094.1:p.Met2388=
XM_017029606.2:c.7135_7137delinsATG	XP_016885095.1:p.Met2379=
XM_017029607.2:c.7132_7134delinsATG	XP_016885096.1:p.Met2378=
XM_017029608.2:c.7084_7086delinsATG	XP_016885097.1:p.Met2362=
XM_017029609.1:c.7048_7050delinsATG	XP_016885098.1:p.Met2350=
XM_017029610.1:c.7045_7047delinsATG	XP_016885099.1:p.Met2349=
XM_017029611.1:c.7000_7002delinsATG	XP_016885100.1:p.Met2334=
XR_001755700.2:n.7665_7667delinsATG
NM_138270.4:c.7252_7254delinsATG	NP_612114.2:p.Met2418=
NM_000489.6:c.7366_7368delinsATG MANE Select	NP_000480.3:p.Met2456=
NM_138270.5:c.7252_7254delinsATG	NP_612114.2:p.Met2418=