Canonical Allele Identifier: CA2581934947
Gene: ASXL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742553_25742563del , CM000664.2:g.25742553_25742563del GRCh38
NC_000002.11:g.25965422_25965432del , CM000664.1:g.25965422_25965432del GRCh37
NC_000002.10:g.25818926_25818936del NCBI36
NG_052995.1:g.140954_140964del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.3771_3781del ENSP00000337250.5:p.Glu1257AspfsTer19
ENST00000435504.9:c.3774_3784del MANE Select ENSP00000391447.3:p.Glu1258AspfsTer19
ENST00000336112.8:c.3690_3700del ENSP00000337250.4:p.Glu1230AspfsTer19
ENST00000404843.5:c.2223_2233del ENSP00000383920.1:p.Glu741AspfsTer19
ENST00000435504.8:c.3774_3784del ENSP00000391447.3:p.Glu1258AspfsTer19
NM_018263.4:c.3774_3784del NP_060733.4:p.Glu1258AspfsTer19
XM_006712039.2:c.3408_3418del XP_006712102.1:p.Glu1136AspfsTer19
XM_006712040.1:c.2994_3004del XP_006712103.1:p.Glu998AspfsTer19
XM_011532950.1:c.3771_3781del XP_011531252.1:p.Glu1257AspfsTer19
XM_011532951.1:c.3600_3610del XP_011531253.1:p.Glu1200AspfsTer19
NM_018263.5:c.3774_3784del NP_060733.4:p.Glu1258AspfsTer19
XM_006712039.3:c.3408_3418del XP_006712102.1:p.Glu1136AspfsTer19
XM_006712040.2:c.2994_3004del XP_006712103.1:p.Glu998AspfsTer19
XM_011532950.3:c.3771_3781del XP_011531252.1:p.Glu1257AspfsTer19
XM_011532951.2:c.3600_3610del XP_011531253.1:p.Glu1200AspfsTer19
XM_017004430.1:c.2994_3004del XP_016859919.1:p.Glu998AspfsTer19
XM_024452974.1:c.3954_3964del XP_024308742.1:p.Glu1318AspfsTer19
NM_001369346.1:c.3600_3610del NP_001356275.1:p.Glu1200AspfsTer19
NM_001369347.1:c.2994_3004del NP_001356276.1:p.Glu998AspfsTer19
NM_018263.6:c.3774_3784del MANE Select NP_060733.4:p.Glu1258AspfsTer19