Canonical Allele Identifier: CA1239490507

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742509T= , CM000664.2:g.25742509T=	GRCh38
NC_000002.11:g.25965378T= , CM000664.1:g.25965378T=	GRCh37
NC_000002.10:g.25818882T=	NCBI36
NG_052995.1:g.141008A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3825A=	ENSP00000337250.5:p.Ala1275=
ENST00000435504.9:c.3828A= MANE Select	ENSP00000391447.3:p.Ala1276=
ENST00000336112.8:c.3744A=	ENSP00000337250.4:p.Ala1248=
ENST00000404843.5:c.2277A=	ENSP00000383920.1:p.Ala759=
ENST00000435504.8:c.3828A=	ENSP00000391447.3:p.Ala1276=
NM_018263.4:c.3828A=	NP_060733.4:p.Ala1276=
XM_006712039.2:c.3462A=	XP_006712102.1:p.Ala1154=
XM_006712040.1:c.3048A=	XP_006712103.1:p.Ala1016=
XM_011532950.1:c.3825A=	XP_011531252.1:p.Ala1275=
XM_011532951.1:c.3654A=	XP_011531253.1:p.Ala1218=
NM_018263.5:c.3828A=	NP_060733.4:p.Ala1276=
XM_006712039.3:c.3462A=	XP_006712102.1:p.Ala1154=
XM_006712040.2:c.3048A=	XP_006712103.1:p.Ala1016=
XM_011532950.3:c.3825A=	XP_011531252.1:p.Ala1275=
XM_011532951.2:c.3654A=	XP_011531253.1:p.Ala1218=
XM_017004430.1:c.3048A=	XP_016859919.1:p.Ala1016=
XM_024452974.1:c.4008A=	XP_024308742.1:p.Ala1336=
NM_001369346.1:c.3654A=	NP_001356275.1:p.Ala1218=
NM_001369347.1:c.3048A=	NP_001356276.1:p.Ala1016=
NM_018263.6:c.3828A= MANE Select	NP_060733.4:p.Ala1276=