Canonical Allele Identifier: CA1239490515

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742536C= , CM000664.2:g.25742536C=	GRCh38
NC_000002.11:g.25965405C= , CM000664.1:g.25965405C=	GRCh37
NC_000002.10:g.25818909C=	NCBI36
NG_052995.1:g.140981G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3798G=	ENSP00000337250.5:p.Gln1266=
ENST00000435504.9:c.3801G= MANE Select	ENSP00000391447.3:p.Gln1267=
ENST00000336112.8:c.3717G=	ENSP00000337250.4:p.Gln1239=
ENST00000404843.5:c.2250G=	ENSP00000383920.1:p.Gln750=
ENST00000435504.8:c.3801G=	ENSP00000391447.3:p.Gln1267=
NM_018263.4:c.3801G=	NP_060733.4:p.Gln1267=
XM_006712039.2:c.3435G=	XP_006712102.1:p.Gln1145=
XM_006712040.1:c.3021G=	XP_006712103.1:p.Gln1007=
XM_011532950.1:c.3798G=	XP_011531252.1:p.Gln1266=
XM_011532951.1:c.3627G=	XP_011531253.1:p.Gln1209=
NM_018263.5:c.3801G=	NP_060733.4:p.Gln1267=
XM_006712039.3:c.3435G=	XP_006712102.1:p.Gln1145=
XM_006712040.2:c.3021G=	XP_006712103.1:p.Gln1007=
XM_011532950.3:c.3798G=	XP_011531252.1:p.Gln1266=
XM_011532951.2:c.3627G=	XP_011531253.1:p.Gln1209=
XM_017004430.1:c.3021G=	XP_016859919.1:p.Gln1007=
XM_024452974.1:c.3981G=	XP_024308742.1:p.Gln1327=
NM_001369346.1:c.3627G=	NP_001356275.1:p.Gln1209=
NM_001369347.1:c.3021G=	NP_001356276.1:p.Gln1007=
NM_018263.6:c.3801G= MANE Select	NP_060733.4:p.Gln1267=