Canonical Allele Identifier: CA1239490428

Gene: ASXL2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742366C= , CM000664.2:g.25742366C=	GRCh38
NC_000002.11:g.25965235C= , CM000664.1:g.25965235C=	GRCh37
NC_000002.10:g.25818739C=	NCBI36
NG_052995.1:g.141151G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3968G=	ENSP00000337250.5:p.Gly1323=
ENST00000435504.9:c.3971G= MANE Select	ENSP00000391447.3:p.Gly1324=
ENST00000336112.8:c.3887G=	ENSP00000337250.4:p.Gly1296=
ENST00000404843.5:c.2420G=	ENSP00000383920.1:p.Gly807=
ENST00000435504.8:c.3971G=	ENSP00000391447.3:p.Gly1324=
NM_018263.4:c.3971G=	NP_060733.4:p.Gly1324=
XM_006712039.2:c.3605G=	XP_006712102.1:p.Gly1202=
XM_006712040.1:c.3191G=	XP_006712103.1:p.Gly1064=
XM_011532950.1:c.3968G=	XP_011531252.1:p.Gly1323=
XM_011532951.1:c.3797G=	XP_011531253.1:p.Gly1266=
NM_018263.5:c.3971G=	NP_060733.4:p.Gly1324=
XM_006712039.3:c.3605G=	XP_006712102.1:p.Gly1202=
XM_006712040.2:c.3191G=	XP_006712103.1:p.Gly1064=
XM_011532950.3:c.3968G=	XP_011531252.1:p.Gly1323=
XM_011532951.2:c.3797G=	XP_011531253.1:p.Gly1266=
XM_017004430.1:c.3191G=	XP_016859919.1:p.Gly1064=
XM_024452974.1:c.4151G=	XP_024308742.1:p.Gly1384=
NM_001369346.1:c.3797G=	NP_001356275.1:p.Gly1266=
NM_001369347.1:c.3191G=	NP_001356276.1:p.Gly1064=
NM_018263.6:c.3971G= MANE Select	NP_060733.4:p.Gly1324=