Canonical Allele Identifier: CA1239490352

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742172C= , CM000664.2:g.25742172C=	GRCh38
NC_000002.11:g.25965041C= , CM000664.1:g.25965041C=	GRCh37
NC_000002.10:g.25818545C=	NCBI36
NG_052995.1:g.141345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4162G=	ENSP00000337250.5:p.Glu1388=
ENST00000435504.9:c.4165G= MANE Select	ENSP00000391447.3:p.Glu1389=
ENST00000336112.8:c.4081G=	ENSP00000337250.4:p.Glu1361=
ENST00000404843.5:c.2614G=	ENSP00000383920.1:p.Glu872=
ENST00000435504.8:c.4165G=	ENSP00000391447.3:p.Glu1389=
NM_018263.4:c.4165G=	NP_060733.4:p.Glu1389=
XM_006712039.2:c.3799G=	XP_006712102.1:p.Glu1267=
XM_006712040.1:c.3385G=	XP_006712103.1:p.Glu1129=
XM_011532950.1:c.4162G=	XP_011531252.1:p.Glu1388=
XM_011532951.1:c.3991G=	XP_011531253.1:p.Glu1331=
NM_018263.5:c.4165G=	NP_060733.4:p.Glu1389=
XM_006712039.3:c.3799G=	XP_006712102.1:p.Glu1267=
XM_006712040.2:c.3385G=	XP_006712103.1:p.Glu1129=
XM_011532950.3:c.4162G=	XP_011531252.1:p.Glu1388=
XM_011532951.2:c.3991G=	XP_011531253.1:p.Glu1331=
XM_017004430.1:c.3385G=	XP_016859919.1:p.Glu1129=
XM_024452974.1:c.4345G=	XP_024308742.1:p.Glu1449=
NM_001369346.1:c.3991G=	NP_001356275.1:p.Glu1331=
NM_001369347.1:c.3385G=	NP_001356276.1:p.Glu1129=
NM_018263.6:c.4165G= MANE Select	NP_060733.4:p.Glu1389=