Canonical Allele Identifier: CA1239490464

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742426T= , CM000664.2:g.25742426T=	GRCh38
NC_000002.11:g.25965295T= , CM000664.1:g.25965295T=	GRCh37
NC_000002.10:g.25818799T=	NCBI36
NG_052995.1:g.141091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3908A=	ENSP00000337250.5:p.Gln1303=
ENST00000435504.9:c.3911A= MANE Select	ENSP00000391447.3:p.Gln1304=
ENST00000336112.8:c.3827A=	ENSP00000337250.4:p.Gln1276=
ENST00000404843.5:c.2360A=	ENSP00000383920.1:p.Gln787=
ENST00000435504.8:c.3911A=	ENSP00000391447.3:p.Gln1304=
NM_018263.4:c.3911A=	NP_060733.4:p.Gln1304=
XM_006712039.2:c.3545A=	XP_006712102.1:p.Gln1182=
XM_006712040.1:c.3131A=	XP_006712103.1:p.Gln1044=
XM_011532950.1:c.3908A=	XP_011531252.1:p.Gln1303=
XM_011532951.1:c.3737A=	XP_011531253.1:p.Gln1246=
NM_018263.5:c.3911A=	NP_060733.4:p.Gln1304=
XM_006712039.3:c.3545A=	XP_006712102.1:p.Gln1182=
XM_006712040.2:c.3131A=	XP_006712103.1:p.Gln1044=
XM_011532950.3:c.3908A=	XP_011531252.1:p.Gln1303=
XM_011532951.2:c.3737A=	XP_011531253.1:p.Gln1246=
XM_017004430.1:c.3131A=	XP_016859919.1:p.Gln1044=
XM_024452974.1:c.4091A=	XP_024308742.1:p.Gln1364=
NM_001369346.1:c.3737A=	NP_001356275.1:p.Gln1246=
NM_001369347.1:c.3131A=	NP_001356276.1:p.Gln1044=
NM_018263.6:c.3911A= MANE Select	NP_060733.4:p.Gln1304=