Canonical Allele Identifier: CA1239490481

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742455A= , CM000664.2:g.25742455A=	GRCh38
NC_000002.11:g.25965324A= , CM000664.1:g.25965324A=	GRCh37
NC_000002.10:g.25818828A=	NCBI36
NG_052995.1:g.141062T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3879T=	ENSP00000337250.5:p.Leu1293=
ENST00000435504.9:c.3882T= MANE Select	ENSP00000391447.3:p.Leu1294=
ENST00000336112.8:c.3798T=	ENSP00000337250.4:p.Leu1266=
ENST00000404843.5:c.2331T=	ENSP00000383920.1:p.Leu777=
ENST00000435504.8:c.3882T=	ENSP00000391447.3:p.Leu1294=
NM_018263.4:c.3882T=	NP_060733.4:p.Leu1294=
XM_006712039.2:c.3516T=	XP_006712102.1:p.Leu1172=
XM_006712040.1:c.3102T=	XP_006712103.1:p.Leu1034=
XM_011532950.1:c.3879T=	XP_011531252.1:p.Leu1293=
XM_011532951.1:c.3708T=	XP_011531253.1:p.Leu1236=
NM_018263.5:c.3882T=	NP_060733.4:p.Leu1294=
XM_006712039.3:c.3516T=	XP_006712102.1:p.Leu1172=
XM_006712040.2:c.3102T=	XP_006712103.1:p.Leu1034=
XM_011532950.3:c.3879T=	XP_011531252.1:p.Leu1293=
XM_011532951.2:c.3708T=	XP_011531253.1:p.Leu1236=
XM_017004430.1:c.3102T=	XP_016859919.1:p.Leu1034=
XM_024452974.1:c.4062T=	XP_024308742.1:p.Leu1354=
NM_001369346.1:c.3708T=	NP_001356275.1:p.Leu1236=
NM_001369347.1:c.3102T=	NP_001356276.1:p.Leu1034=
NM_018263.6:c.3882T= MANE Select	NP_060733.4:p.Leu1294=