Canonical Allele Identifier: CA1239490508

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742512A= , CM000664.2:g.25742512A=	GRCh38
NC_000002.11:g.25965381A= , CM000664.1:g.25965381A=	GRCh37
NC_000002.10:g.25818885A=	NCBI36
NG_052995.1:g.141005T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3822T=	ENSP00000337250.5:p.His1274=
ENST00000435504.9:c.3825T= MANE Select	ENSP00000391447.3:p.His1275=
ENST00000336112.8:c.3741T=	ENSP00000337250.4:p.His1247=
ENST00000404843.5:c.2274T=	ENSP00000383920.1:p.His758=
ENST00000435504.8:c.3825T=	ENSP00000391447.3:p.His1275=
NM_018263.4:c.3825T=	NP_060733.4:p.His1275=
XM_006712039.2:c.3459T=	XP_006712102.1:p.His1153=
XM_006712040.1:c.3045T=	XP_006712103.1:p.His1015=
XM_011532950.1:c.3822T=	XP_011531252.1:p.His1274=
XM_011532951.1:c.3651T=	XP_011531253.1:p.His1217=
NM_018263.5:c.3825T=	NP_060733.4:p.His1275=
XM_006712039.3:c.3459T=	XP_006712102.1:p.His1153=
XM_006712040.2:c.3045T=	XP_006712103.1:p.His1015=
XM_011532950.3:c.3822T=	XP_011531252.1:p.His1274=
XM_011532951.2:c.3651T=	XP_011531253.1:p.His1217=
XM_017004430.1:c.3045T=	XP_016859919.1:p.His1015=
XM_024452974.1:c.4005T=	XP_024308742.1:p.His1335=
NM_001369346.1:c.3651T=	NP_001356275.1:p.His1217=
NM_001369347.1:c.3045T=	NP_001356276.1:p.His1015=
NM_018263.6:c.3825T= MANE Select	NP_060733.4:p.His1275=