Canonical Allele Identifier: CA1239490525

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742570A= , CM000664.2:g.25742570A=	GRCh38
NC_000002.11:g.25965439A= , CM000664.1:g.25965439A=	GRCh37
NC_000002.10:g.25818943A=	NCBI36
NG_052995.1:g.140947T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3764T=	ENSP00000337250.5:p.Phe1255=
ENST00000435504.9:c.3767T= MANE Select	ENSP00000391447.3:p.Phe1256=
ENST00000336112.8:c.3683T=	ENSP00000337250.4:p.Phe1228=
ENST00000404843.5:c.2216T=	ENSP00000383920.1:p.Phe739=
ENST00000435504.8:c.3767T=	ENSP00000391447.3:p.Phe1256=
NM_018263.4:c.3767T=	NP_060733.4:p.Phe1256=
XM_006712039.2:c.3401T=	XP_006712102.1:p.Phe1134=
XM_006712040.1:c.2987T=	XP_006712103.1:p.Phe996=
XM_011532950.1:c.3764T=	XP_011531252.1:p.Phe1255=
XM_011532951.1:c.3593T=	XP_011531253.1:p.Phe1198=
NM_018263.5:c.3767T=	NP_060733.4:p.Phe1256=
XM_006712039.3:c.3401T=	XP_006712102.1:p.Phe1134=
XM_006712040.2:c.2987T=	XP_006712103.1:p.Phe996=
XM_011532950.3:c.3764T=	XP_011531252.1:p.Phe1255=
XM_011532951.2:c.3593T=	XP_011531253.1:p.Phe1198=
XM_017004430.1:c.2987T=	XP_016859919.1:p.Phe996=
XM_024452974.1:c.3947T=	XP_024308742.1:p.Phe1316=
NM_001369346.1:c.3593T=	NP_001356275.1:p.Phe1198=
NM_001369347.1:c.2987T=	NP_001356276.1:p.Phe996=
NM_018263.6:c.3767T= MANE Select	NP_060733.4:p.Phe1256=